A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6346673



Internal ID21004226
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:182912721..182913497hg38UCSC Ensembl
chr2:183777449..183778225hg19UCSC Ensembl
Cytoband2q32.1
Allele length
AssemblyAllele length
hg38777
hg19777
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18081636
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6346673
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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