A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17412019



Internal ID22469889
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:160704914..160704914hg38UCSC Ensembl
chr5:160131921..160131921hg19UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg38255
hg19255
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5963122
Supporting Variants
Samples
Known GenesATP10B
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17412019
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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