A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6356642



Internal ID21014195
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:122766581..122768691hg38UCSC Ensembl
chr3:122485428..122487538hg19UCSC Ensembl
Cytoband3q21.1
Allele length
AssemblyAllele length
hg382111
hg192111
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18095213
Samples
Known GenesHSPBAP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6356642
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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