A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6361829



Internal ID21019382
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:124250782..124252351hg38UCSC Ensembl
chr3:123969629..123971198hg19UCSC Ensembl
Cytoband3q21.2
Allele length
AssemblyAllele length
hg381570
hg191570
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18093389
Samples
Known GenesKALRN
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6361829
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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