A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17030251



Internal ID87880
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:13233314..13234242hg38UCSC Ensembl
chr10:13275314..13276242hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg38929
hg19929
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5490272
Supporting Variants
Samples
Known GenesUCMA
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17030251
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.002342


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