A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv999463



Internal ID18812313
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:204799832..204858913hg38UCSC Ensembl
Innerchr1:204768960..204828041hg19UCSC Ensembl
Innerchr1:203035583..203094664hg18UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg3859082
hg1959082
hg1859082
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3500263
Samples
Known GenesNFASC
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv999463
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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