A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1021917



Internal ID19111135
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:45911327..45930577hg38UCSC Ensembl
Innerchr6:45879064..45898314hg19UCSC Ensembl
Innerchr6:45987042..46006292hg18UCSC Ensembl
Cytoband6p12.3
Allele length
AssemblyAllele length
hg3819251
hg1919251
hg1819251
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3657441
Samples
Known GenesCLIC5
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1021917
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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