A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6370950



Internal ID21028503
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:183680805..183681430hg38UCSC Ensembl
chr3:183398593..183399218hg19UCSC Ensembl
Cytoband3q27.1
Allele length
AssemblyAllele length
hg38626
hg19626
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18097557
Samples
Known GenesKLHL24
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6370950
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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