A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17592014



Internal ID21784057
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:12335606..12336177hg38UCSC Ensembl
chr10:12377605..12378176hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg38572
hg19572
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6000868
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17592014
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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