A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6349920



Internal ID21007473
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:72500722..72501161hg38UCSC Ensembl
chr2:72727851..72728290hg19UCSC Ensembl
Cytoband2p13.2
Allele length
AssemblyAllele length
hg38440
hg19440
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18089669
Samples
Known GenesEXOC6B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6349920
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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