A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6504174



Internal ID20877435
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 StatusM
Merged Variants
Supporting Variantsnssv18034250
Samples
Known GenesCDRT15L2, KRT16P3, LGALS9B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6504174
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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