A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6418831



Internal ID21076384
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:19989370..20063504hg38UCSC Ensembl
chr9:19989368..20063502hg19UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg3874135
hg1974135
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7640n223
Supporting Variantsnssv18175611
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6418831
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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