A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6493634



Internal ID21151187
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:41755276..41755692hg38UCSC Ensembl
chr13:42329412..42329828hg19UCSC Ensembl
Cytoband13q14.11
Allele length
AssemblyAllele length
hg38417
hg19417
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18009581
Samples
Known GenesVWA8
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6493634
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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