A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv701202



Internal ID15437854
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:106292704..106296034hg38UCSC Ensembl
Innerchr3:106011551..106014881hg19UCSC Ensembl
Innerchr3:107494241..107497571hg18UCSC Ensembl
Innerchr3:107494241..107497571hg17UCSC Ensembl
Cytoband3q13.11
Allele length
AssemblyAllele length
hg383331
hg193331
hg183331
hg173331
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv525134
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv701202
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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