A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17581346



Internal ID21773389
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:116984533..116984601hg38UCSC Ensembl
chr10:118744044..118744112hg19UCSC Ensembl
Cytoband10q25.3
Allele length
AssemblyAllele length
hg3869
hg1969
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6015098
Supporting Variants
Samples
Known GenesKIAA1598
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17581346
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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