A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17536661



Internal ID21861016
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:15063839..15063897hg38UCSC Ensembl
chr1:15390335..15390393hg19UCSC Ensembl
Cytoband1p36.21
Allele length
AssemblyAllele length
hg3859
hg1959
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5981435
Supporting Variants
Samples
Known GenesKAZN
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17536661
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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