A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17712005



Internal ID135671
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:19493944..19496503hg38UCSC Ensembl
chr17:19397257..19399816hg19UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg382560
hg192560
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5514770
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17712005
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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