A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6337330



Internal ID20994883
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:158581675..158586564hg38UCSC Ensembl
chr2:159438187..159443076hg19UCSC Ensembl
Cytoband2q24.1
Allele length
AssemblyAllele length
hg384890
hg194890
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18079869
Samples
Known GenesPKP4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6337330
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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