A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6357372



Internal ID21014925
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:46611760..46613399hg38UCSC Ensembl
chr3:46653250..46654889hg19UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg381640
hg191640
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18100717
Samples
Known GenesLOC100132146
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6357372
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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