A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17685971



Internal ID109637
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:20678951..20683881hg38UCSC Ensembl
chr13:21253090..21258020hg19UCSC Ensembl
Cytoband13q12.11
Allele length
AssemblyAllele length
hg384931
hg194931
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5494168
Supporting Variants
Samples
Known GenesIFT88
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17685971
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000625


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