A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3591820



Internal ID18890101
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:6599013..6611633hg38UCSC Ensembl
Innerchr3:6640700..6653320hg19UCSC Ensembl
Innerchr3:6615700..6628320hg18UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg3812621
hg1912621
hg1812621
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1005576
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3591820
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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