A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv664620



Internal ID15401272
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:149761534..149831173hg38UCSC Ensembl
Innerchr7:149458623..149528262hg19UCSC Ensembl
Innerchr7:149089556..149159195hg18UCSC Ensembl
Innerchr7:148896271..148965910hg17UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg3869640
hg1969640
hg1869640
hg1769640
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517242
Supporting Variants
Samples
Known GenesSSPO, ZNF467
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv664620
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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