A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6358046



Internal ID21015599
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:113751304..113766494hg38UCSC Ensembl
chr3:113470151..113485341hg19UCSC Ensembl
Cytoband3q13.2
Allele length
AssemblyAllele length
hg3815191
hg1915191
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18093157
Samples
Known GenesATP6V1A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6358046
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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