A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6372241



Internal ID21029794
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:186246202..186250729hg38UCSC Ensembl
chr3:185963991..185968518hg19UCSC Ensembl
Cytoband3q27.2
Allele length
AssemblyAllele length
hg384528
hg194528
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18100499
Samples
Known GenesDGKG
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6372241
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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