A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6349930



Internal ID21007483
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:191490546..191500173hg38UCSC Ensembl
chr2:192355272..192364899hg19UCSC Ensembl
Cytoband2q32.3
Allele length
AssemblyAllele length
hg389628
hg199628
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18081449
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6349930
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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