A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1051650



Internal ID15558150
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:27688476..27762285hg38UCSC Ensembl
Innerchr6:27656255..27730064hg19UCSC Ensembl
Innerchr6:27764234..27838043hg18UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg3873810
hg1973810
hg1873810
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv601205
Supporting Variants
Samples
Known GenesLINC01012, LOC100131289
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1051650
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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