A curated catalogue of human genomic structural variation




Variant Details

Variant: essv12917616



Internal ID689214
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:106628393..106629183hg38UCSC Ensembl
Innerchr7:106628529..106629033hg38UCSC Ensembl
Outerchr7:106628194..106629382hg38UCSC Ensembl
chr7:106268839..106269629hg19UCSC Ensembl
Innerchr7:106268975..106269479hg19UCSC Ensembl
Outerchr7:106268640..106269828hg19UCSC Ensembl
Cytoband7q22.3
Allele length
AssemblyAllele length
hg38791
hg19791
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3614446
Supporting Variants
SamplesHG00324
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv12917616
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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