A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6345077



Internal ID21002630
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:85645415..85650224hg38UCSC Ensembl
chr2:85872538..85877347hg19UCSC Ensembl
Cytoband2p11.2
Allele length
AssemblyAllele length
hg384810
hg194810
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18091143
Samples
Known GenesUSP39
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6345077
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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