A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3495760



Internal ID18736715
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:184614071..184640686hg38UCSC Ensembl
Innerchr1:184583205..184609820hg19UCSC Ensembl
Innerchr1:182849828..182876443hg18UCSC Ensembl
Cytoband1q25.3
Allele length
AssemblyAllele length
hg3826616
hg1926616
hg1826616
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1008237
Supporting Variants
Samples
Known GenesC1orf21
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3495760
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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