A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6343546



Internal ID21001099
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:187577643..187676832hg38UCSC Ensembl
chr2:188442370..188541559hg19UCSC Ensembl
Cytoband2q32.1
Allele length
AssemblyAllele length
hg3899190
hg1999190
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4220n223
Supporting Variantsnssv18080821
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6343546
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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