A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6356231



Internal ID21013784
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:62512901..62546300hg38UCSC Ensembl
chr3:62498576..62531975hg19UCSC Ensembl
Cytoband3p14.2
Allele length
AssemblyAllele length
hg3833400
hg1933400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4892n223
Supporting Variantsnssv18101776
Samples
Known GenesCADPS
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6356231
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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