A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6320364



Internal ID20853462
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:46310868..46313375hg38UCSC Ensembl
chr1:46776540..46779047hg19UCSC Ensembl
Cytoband1p34.1
Allele length
AssemblyAllele length
hg382508
hg192508
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18061137
Samples
Known GenesUQCRH
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6320364
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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