A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17029080



Internal ID87083
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:8216221..8216280hg38UCSC Ensembl
chr10:8258184..8258243hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5480531
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17029080
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000625


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