A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv705363



Internal ID15442015
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:133718934..133731527hg38UCSC Ensembl
Innerchr3:133437778..133450371hg19UCSC Ensembl
Innerchr3:134920468..134933061hg18UCSC Ensembl
Innerchr3:134920476..134933069hg17UCSC Ensembl
Cytoband3q22.1
Allele length
AssemblyAllele length
hg3812594
hg1912594
hg1812594
hg1712594
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv528713
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv705363
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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