A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17035235



Internal ID91226
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:71302500..71302603hg38UCSC Ensembl
chr10:73062257..73062360hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg38104
hg19104
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6144264
Supporting Variants
Samples
Known GenesUNC5B
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17035235
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.003126


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