A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv703876



Internal ID15440528
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:148422604..148446350hg38UCSC Ensembl
Innerchr7:148119696..148143442hg19UCSC Ensembl
Innerchr7:147750629..147774375hg18UCSC Ensembl
Innerchr7:147557344..147581090hg17UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg3823747
hg1923747
hg1823747
hg1723747
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv527436
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv703876
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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