A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17033380



Internal ID89944
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:28153208..28157094hg38UCSC Ensembl
chr10:28442137..28446023hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg383887
hg193887
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5484417
Supporting Variants
Samples
Known GenesMPP7
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17033380
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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