A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1025846



Internal ID19115063
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:45987436..46079532hg38UCSC Ensembl
Innerchr6:45955173..46047269hg19UCSC Ensembl
Innerchr6:46063132..46155228hg18UCSC Ensembl
Cytoband6p12.3
Allele length
AssemblyAllele length
hg3892097
hg1992097
hg1892097
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3657442
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)nsv1025846
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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