A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17029065



Internal ID87074
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:8062522..8062582hg38UCSC Ensembl
chr10:8104485..8104545hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5487071
Supporting Variants
Samples
Known GenesGATA3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17029065
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000468


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