A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv611350



Internal ID16398759
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:50971367..51277236hg38UCSC Ensembl
Innerchr8:51883927..52189796hg19UCSC Ensembl
Innerchr8:52046480..52352349hg18UCSC Ensembl
Cytoband8q11.21
Allele length
AssemblyAllele length
hg38305870
hg19305870
hg18305870
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1156831
Samples1780862345_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv611350
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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