A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6347306



Internal ID21004859
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:239182601..239184900hg38UCSC Ensembl
chr2:240104297..240106596hg19UCSC Ensembl
Cytoband2q37.3
Allele length
AssemblyAllele length
hg382300
hg192300
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18084477
Samples
Known GenesHDAC4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6347306
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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