A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6357613



Internal ID21015166
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:186311702..186312123hg38UCSC Ensembl
chr3:186029491..186029912hg19UCSC Ensembl
Cytoband3q27.3
Allele length
AssemblyAllele length
hg38422
hg19422
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18099510
Samples
Known GenesDGKG
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6357613
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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