A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1071960



Internal ID15925146
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:108805722..108883586hg38UCSC Ensembl
Innerchr6:109126925..109204789hg19UCSC Ensembl
Innerchr6:109233618..109311482hg18UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg3877865
hg1977865
hg1877865
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv604483
Supporting Variants
Samples
Known GenesARMC2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1071960
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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