A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6423883



Internal ID21081436
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:15501833..15504350hg38UCSC Ensembl
chr9:15501831..15504348hg19UCSC Ensembl
Cytoband9p22.3
Allele length
AssemblyAllele length
hg382518
hg192518
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18175656
Samples
Known GenesPSIP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6423883
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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