A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6351344



Internal ID21008897
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:191548008..191552713hg38UCSC Ensembl
chr2:192412734..192417439hg19UCSC Ensembl
Cytoband2q32.3
Allele length
AssemblyAllele length
hg384706
hg194706
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18081453
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6351344
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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