A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6073237



Internal ID21982470
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:160109782..160109782hg38UCSC Ensembl
chr5:159536789..159536789hg19UCSC Ensembl
Cytoband5q33.3
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17576908
Samples
Known GenesPWWP2A
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6073237
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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