A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4018552



Internal ID22080183
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:37995532..38018691hg38UCSC Ensembl
Outerchr6:37993807..38020088hg38UCSC Ensembl
Innerchr6:37963308..37986467hg19UCSC Ensembl
Outerchr6:37961583..37987864hg19UCSC Ensembl
Cytoband6p21.2
Allele length
AssemblyAllele length
hg3826282
hg1926282
Variant TypeCNV duplication
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1156495
Supporting Variants
Samples
Known GenesZFAND3
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4018552
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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