A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6341156



Internal ID20998709
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:193006028..193227114hg38UCSC Ensembl
chr2:193870754..194091840hg19UCSC Ensembl
Cytoband2q32.3
Allele length
AssemblyAllele length
hg38221087
hg19221087
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4237n223
Supporting Variantsnssv18081209
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6341156
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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