A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17612062



Internal ID21804109
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:90499376..90499479hg38UCSC Ensembl
chr15:91042608..91042711hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg38104
hg19104
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6022174
Supporting Variants
Samples
Known GenesIQGAP1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17612062
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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