A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6372699



Internal ID21030252
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:132000028..132000722hg38UCSC Ensembl
chr3:131718872..131719566hg19UCSC Ensembl
Cytoband3q22.1
Allele length
AssemblyAllele length
hg38695
hg19695
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18095295
Samples
Known GenesCPNE4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6372699
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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