A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3636805



Internal ID7023599
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:68458402..68464929hg38UCSC Ensembl
Innerchr15:68458402..68464929hg38UCSC Ensembl
Outerchr15:68458163..68465155hg38UCSC Ensembl
chr15:68750741..68757268hg19UCSC Ensembl
Innerchr15:68750741..68757268hg19UCSC Ensembl
Outerchr15:68750502..68757494hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg386528
hg196528
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15279456, essv15279457, essv15279458, essv15279455
SamplesHG01521, NA11994, HG01447, HG01464
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3636805
Frequency
Sample Size2504
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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