A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3952901



Internal ID21372970
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:137686873..137688197hg38UCSC Ensembl
chr5:137022562..137023886hg19UCSC Ensembl
Cytoband5q31.2
Allele length
AssemblyAllele length
hg381325
hg191325
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15196931
SamplesHG002
Known GenesKLHL3
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3952901
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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