A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6365781



Internal ID21023334
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:140109397..140109838hg38UCSC Ensembl
chr3:139828239..139828680hg19UCSC Ensembl
Cytoband3q23
Allele length
AssemblyAllele length
hg38442
hg19442
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18093977
Samples
Known GenesCLSTN2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6365781
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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