A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1061236



Internal ID15914422
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:62576461..62886207hg38UCSC Ensembl
Innerchr6:63286366..63596112hg19UCSC Ensembl
Innerchr6:63344325..63654071hg18UCSC Ensembl
Cytoband6q11.1
Allele length
AssemblyAllele length
hg38309747
hg19309747
hg18309747
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv603352
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1061236
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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