A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3749567



Internal ID19047848
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:160603885..160647998hg38UCSC Ensembl
Innerchr6:161024917..161069030hg19UCSC Ensembl
Innerchr6:160944907..160989020hg18UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg3844114
hg1944114
hg1844114
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1030067
Supporting Variants
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)nssv3749567
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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