A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6368773



Internal ID21026326
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:143045588..143365340hg38UCSC Ensembl
chr3:142764430..143084182hg19UCSC Ensembl
Cytoband3q23
Allele length
AssemblyAllele length
hg38319753
hg19319753
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18209670
Samples
Known GenesCHST2, SLC9A9, SLC9A9-AS1, U2SURP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6368773
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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