A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1154842



Internal ID15880422
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:81075186..81183608hg38UCSC Ensembl
Innerchr6:81784903..81893325hg19UCSC Ensembl
Innerchr6:81841622..81950044hg18UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg38108423
hg19108423
hg18108423
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv604086
Supporting Variants
SamplesNINDS_208
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1154842
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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