A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1072053



Internal ID15925239
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:113136525..113379521hg38UCSC Ensembl
Innerchr6:113457727..113700723hg19UCSC Ensembl
Innerchr6:113564420..113807416hg18UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg38242997
hg19242997
hg18242997
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv604518
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)nssv1072053
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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