A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17565137



Internal ID21889492
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:160635245..160635245hg38UCSC Ensembl
chr5:160062252..160062252hg19UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg38127
hg19127
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6069250
Supporting Variants
Samples
Known GenesATP10B
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17565137
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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