A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3649841



Internal ID18948122
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:95898757..95939915hg38UCSC Ensembl
Innerchr6:96346633..96387791hg19UCSC Ensembl
Innerchr6:96453354..96494512hg18UCSC Ensembl
Cytoband6q16.1
Allele length
AssemblyAllele length
hg3841159
hg1941159
hg1841159
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1021442
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3649841
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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