A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv691888



Internal ID15081854
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:155454197..155465199hg38UCSC Ensembl
Innerchr7:155246892..155257894hg19UCSC Ensembl
Innerchr7:154939653..154950655hg18UCSC Ensembl
Innerchr7:154746368..154757370hg17UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg3811003
hg1911003
hg1811003
hg1711003
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv520626
Supporting Variants
Samples
Known GenesEN2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv691888
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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