A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17036885



Internal ID92346
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:91310585..91316359hg38UCSC Ensembl
chr10:93070342..93076116hg19UCSC Ensembl
Cytoband10q23.32
Allele length
AssemblyAllele length
hg385775
hg195775
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5481847
Supporting Variants
Samples
Known GenesLOC100188947
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17036885
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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