A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6359604



Internal ID21017157
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:119410718..119412235hg38UCSC Ensembl
chr3:119129565..119131082hg19UCSC Ensembl
Cytoband3q13.33
Allele length
AssemblyAllele length
hg381518
hg191518
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18094550
Samples
Known GenesARHGAP31
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6359604
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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