A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3464356



Internal ID19060657
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:2796762..2924777hg38UCSC Ensembl
Innerchr1:2713327..2841342hg19UCSC Ensembl
Innerchr1:2703187..2831202hg18UCSC Ensembl
Cytoband1p36.32
Allele length
AssemblyAllele length
hg38128016
hg19128016
hg18128016
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv997701
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)nssv3464356
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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