A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17712089



Internal ID135755
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:20472055..20702000hg38UCSC Ensembl
chr17:20375368..20605313hg19UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg38229946
hg19229946
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5521702
Supporting Variants
Samples
Known GenesCDRT15L2, KRT16P3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17712089
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.001093


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