A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1017965



Internal ID19107182
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:160605155..160647502hg38UCSC Ensembl
Innerchr6:161026187..161068534hg19UCSC Ensembl
Innerchr6:160946177..160988524hg18UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg3842348
hg1942348
hg1842348
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6166n100
Supporting Variantsnssv3654497
Samples
Known GenesLPA
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1017965
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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