A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv703449



Internal ID15440101
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:131603903..131606035hg38UCSC Ensembl
Innerchr7:131288662..131290794hg19UCSC Ensembl
Innerchr7:130939202..130941334hg18UCSC Ensembl
Innerchr7:130745917..130748049hg17UCSC Ensembl
Cytoband7q32.3
Allele length
AssemblyAllele length
hg382133
hg192133
hg182133
hg172133
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv527070
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv703449
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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