A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6423530



Internal ID21081083
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:19106686..19110515hg38UCSC Ensembl
chr9:19106684..19110513hg19UCSC Ensembl
Cytoband9p22.1
Allele length
AssemblyAllele length
hg383830
hg193830
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18175534
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6423530
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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