A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6370295



Internal ID21027848
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:156027124..156079392hg38UCSC Ensembl
chr3:155744913..155797181hg19UCSC Ensembl
Cytoband3q25.31
Allele length
AssemblyAllele length
hg3852269
hg1952269
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18209750
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6370295
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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