A curated catalogue of human genomic structural variation




Variant Details

Variant: essv12685958



Internal ID1077414
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:15122724..15207056hg38UCSC Ensembl
Innerchr7:15122741..15207040hg38UCSC Ensembl
Outerchr7:15122708..15207073hg38UCSC Ensembl
chr7:15162349..15246681hg19UCSC Ensembl
Innerchr7:15162366..15246665hg19UCSC Ensembl
Outerchr7:15162333..15246698hg19UCSC Ensembl
Cytoband7p21.2
Allele length
AssemblyAllele length
hg3884333
hg1984333
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3612345
Supporting Variants
SamplesHG00701
Known GenesAGMO
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv12685958
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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