A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17595995



Internal ID21788038
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:23790442..23790588hg38UCSC Ensembl
chr10:24079371..24079517hg19UCSC Ensembl
Cytoband10p12.2
Allele length
AssemblyAllele length
hg38147
hg19147
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6012495
Supporting Variants
Samples
Known GenesKIAA1217
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17595995
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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