A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv701972



Internal ID15438624
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:44384499..44420412hg38UCSC Ensembl
Innerchr3:44425991..44461904hg19UCSC Ensembl
Innerchr3:44400995..44436908hg18UCSC Ensembl
Innerchr3:44400995..44436908hg17UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg3835914
hg1935914
hg1835914
hg1735914
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv525792
Supporting Variants
Samples
Known GenesTCAIM
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv701972
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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