A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1024195



Internal ID19113412
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:164624552..164668591hg38UCSC Ensembl
Innerchr6:165045585..165089624hg19UCSC Ensembl
Innerchr6:164965575..165009614hg18UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg3844040
hg1944040
hg1844040
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3749618, nssv3749619
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)nsv1024195
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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