A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3637098



Internal ID7023892
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:84699744..84700547hg38UCSC Ensembl
Innerchr15:84699769..84700522hg38UCSC Ensembl
Outerchr15:84699719..84700572hg38UCSC Ensembl
chr15:85242975..85243778hg19UCSC Ensembl
Innerchr15:85243000..85243753hg19UCSC Ensembl
Outerchr15:85242950..85243803hg19UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg38804
hg19804
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15313653, essv15313633, essv15313641, essv15313663, essv15313659, essv15313664, essv15313655, essv15313647, essv15313658, essv15313635, essv15313654, essv15313631, essv15313634, essv15313645, essv15313648, essv15313639, essv15313657, essv15313660, essv15313632, essv15313656, essv15313638, essv15313644, essv15313649, essv15313662, essv15313637, essv15313652, essv15313643, essv15313646, essv15313665, essv15313651, essv15313640, essv15313650, essv15313642, essv15313636, essv15313661
SamplesHG01986, NA19920, NA19314, NA19107, NA19374, NA18923, NA19023, NA19457, HG02054, NA19404, NA19041, HG01440, NA19159, HG03270, HG02820, HG02678, HG03294, HG02445, NA19257, NA19225, HG02332, HG02772, NA19375, NA19147, NA20351, HG02941, NA19475, HG02646, HG02938, HG02679, HG02052, NA18488, NA19312, HG02805, NA19431
Known GenesSEC11A
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3637098
Frequency
Sample Size2504
Observed Gain0
Observed Loss35
Observed Complex0
Frequencyn/a


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