A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17587012



Internal ID21779055
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:516847..583990hg38UCSC Ensembl
chr10:562787..629930hg19UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg3867144
hg1967144
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6001642
Supporting Variants
Samples
Known GenesDIP2C
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17587012
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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