A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6399200



Internal ID21056753
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:149045464..149045970hg38UCSC Ensembl
chr5:148425027..148425533hg19UCSC Ensembl
Cytoband5q32
Allele length
AssemblyAllele length
hg38507
hg19507
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18126533
Samples
Known GenesSH3TC2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6399200
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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