A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6368261



Internal ID21025814
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:120639288..120642427hg38UCSC Ensembl
chr3:120358135..120361274hg19UCSC Ensembl
Cytoband3q13.33
Allele length
AssemblyAllele length
hg383140
hg193140
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18093596
Samples
Known GenesHGD
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6368261
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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