A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6365800



Internal ID21023353
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:120428309..120428616hg38UCSC Ensembl
chr3:120147156..120147463hg19UCSC Ensembl
Cytoband3q13.33
Allele length
AssemblyAllele length
hg38308
hg19308
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18093581
Samples
Known GenesFSTL1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6365800
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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