A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6353938



Internal ID21011491
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:24035691..24036400hg38UCSC Ensembl
chr2:24258561..24259270hg19UCSC Ensembl
Cytoband2p23.3
Allele length
AssemblyAllele length
hg38710
hg19710
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18084540
Samples
Known GenesC2orf44
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6353938
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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