A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6339539



Internal ID20997092
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:63239750..63352983hg38UCSC Ensembl
chr2:63466885..63580118hg19UCSC Ensembl
Cytoband2p15
Allele length
AssemblyAllele length
hg38113234
hg19113234
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18089220
Samples
Known GenesWDPCP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6339539
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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