A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13039352



Internal ID5981209
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3615666
Supporting Variants
SamplesNA19390
Known GenesLINC00244, LINC01006
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13039352
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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