A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15703601



Internal ID21375877
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:137686874..137688197hg38UCSC Ensembl
chr5:137022563..137023886hg19UCSC Ensembl
Cytoband5q31.2
Allele length
AssemblyAllele length
hg381324
hg191324
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4392129
Supporting Variants
Samples
Known GenesKLHL3
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceWong_et_al_2019
Pubmed ID31340865
Accession Number(s)nssv15703601
Frequency
Sample Size174
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.954023


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