A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv697992



Internal ID15087958
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:155454197..155459499hg38UCSC Ensembl
Innerchr7:155246892..155252194hg19UCSC Ensembl
Innerchr7:154939653..154944955hg18UCSC Ensembl
Innerchr7:154746368..154751670hg17UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg385303
hg195303
hg185303
hg175303
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)nssv697992
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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