A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3608003



Internal ID6994934
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:7063448..7069570hg38UCSC Ensembl
Innerchr6:7063476..7069542hg38UCSC Ensembl
Outerchr6:7063420..7069598hg38UCSC Ensembl
chr6:7063681..7069803hg19UCSC Ensembl
Innerchr6:7063709..7069775hg19UCSC Ensembl
Outerchr6:7063653..7069831hg19UCSC Ensembl
Cytoband6p25.1
Allele length
AssemblyAllele length
hg386123
hg196123
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12182914, essv12182913
SamplesHG01525, NA19072
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3608003
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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