A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3615666



Internal ID7002555
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:156531887..156542864hg38UCSC Ensembl
Innerchr7:156531898..156542854hg38UCSC Ensembl
Outerchr7:156531877..156542875hg38UCSC Ensembl
chr7:156324581..156335558hg19UCSC Ensembl
Innerchr7:156324592..156335548hg19UCSC Ensembl
Outerchr7:156324571..156335569hg19UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg3810978
hg1910978
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13039353, essv13039354, essv13039356, essv13039351, essv13039352, essv13039355
SamplesNA19397, NA19390, HG01894, NA19439, NA19430, NA19463
Known GenesLINC00244, LINC01006
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3615666
Frequency
Sample Size2504
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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