A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6360588



Internal ID21018141
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:186457114..186459754hg38UCSC Ensembl
chr3:186174903..186177543hg19UCSC Ensembl
Cytoband3q27.3
Allele length
AssemblyAllele length
hg382641
hg192641
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18099525
Samples
Known GenesLOC253573
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6360588
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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