A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6480243



Internal ID21137796
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:112958701..112961500hg38UCSC Ensembl
chr13:113613015..113615814hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg382800
hg192800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18007301
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6480243
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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