A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv703405



Internal ID15440057
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:145143631..145148502hg38UCSC Ensembl
Innerchr7:144840724..144845595hg19UCSC Ensembl
Innerchr7:144471657..144476528hg18UCSC Ensembl
Innerchr7:144278372..144283243hg17UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg384872
hg194872
hg184872
hg174872
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv527030
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv703405
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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