A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18034250



Internal ID20601290
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:20467529..20698842hg38UCSC Ensembl
chr17:20370842..20602155hg19UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg38231314
hg19231314
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6504174
Supporting Variants
Samples
Known GenesCDRT15L2, KRT16P3, LGALS9B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18034250
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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