A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3112624



Internal ID21295890
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:159725955..159729776hg38UCSC Ensembl
Innerchr6:160146987..160150808hg19UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg383822
hg193822
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14083163, nssv14082897
Samplessample378, sample304
Known GenesWTAP
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3112624
Frequency
Sample Size467
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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