A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17592968



Internal ID21785011
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:16412653..16412902hg38UCSC Ensembl
chr10:16454652..16454901hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg38250
hg19250
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6020230
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17592968
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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