A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv576864



Internal ID16364273
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:49646360..49691751hg38UCSC Ensembl
Innerchr18:47172730..47218121hg19UCSC Ensembl
Innerchr18:45426728..45472119hg18UCSC Ensembl
Cytoband18q21.1
Allele length
AssemblyAllele length
hg3845392
hg1945392
hg1845392
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1150255
Samples1782681329_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv576864
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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