A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6369057



Internal ID21026610
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:38450397..38451826hg38UCSC Ensembl
chr3:38491888..38493317hg19UCSC Ensembl
Cytoband3p22.2
Allele length
AssemblyAllele length
hg381430
hg191430
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18100832
Samples
Known GenesACVR2B-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6369057
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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