A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17035851



Internal ID91644
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:59745529..59745632hg38UCSC Ensembl
chr10:61505287..61505390hg19UCSC Ensembl
Cytoband10q21.2
Allele length
AssemblyAllele length
hg38104
hg19104
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5490256
Supporting Variants
Samples
Known GenesLINC00948
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17035851
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.010319


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