A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6360991



Internal ID21018544
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:123984066..123984385hg38UCSC Ensembl
chr3:123702913..123703232hg19UCSC Ensembl
Cytoband3q21.1
Allele length
AssemblyAllele length
hg38320
hg19320
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18095262
Samples
Known GenesROPN1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6360991
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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