A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3466523



Internal ID19061798
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:34625845..34638783hg38UCSC Ensembl
Innerchr1:35091446..35104384hg19UCSC Ensembl
Innerchr1:34864033..34876971hg18UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg3812939
hg1912939
hg1812939
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1003697
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)nssv3466523
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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