A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6374924



Internal ID21032477
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:63961094..63964662hg38UCSC Ensembl
chr3:63946770..63950338hg19UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg383569
hg193569
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18101470
Samples
Known GenesATXN7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6374924
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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