A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv662477



Internal ID15399129
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:42504120..42507401hg38UCSC Ensembl
Innerchr7:42543719..42547000hg19UCSC Ensembl
Innerchr7:42510244..42513525hg18UCSC Ensembl
Innerchr7:42316959..42320240hg17UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg383282
hg193282
hg183282
hg173282
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515778
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv662477
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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