A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6341523



Internal ID20999076
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:160110946..160218328hg38UCSC Ensembl
chr2:160967457..161074839hg19UCSC Ensembl
Cytoband2q24.2
Allele length
AssemblyAllele length
hg38107383
hg19107383
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4165n223
Supporting Variantsnssv18205615
Samples
Known GenesITGB6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6341523
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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