A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16976443



Internal ID51684
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:160689845..160690145hg38UCSC Ensembl
chr5:160116852..160117152hg19UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg38301
hg19301
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5556385
Supporting Variants
Samples
Known GenesATP10B
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16976443
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.0064


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