A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14088487



Internal ID21271813
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:37904073..37994204hg38UCSC Ensembl
Innerchr10:38193001..38283132hg19UCSC Ensembl
Cytoband10p11.1
Allele length
AssemblyAllele length
hg3890132
hg1990132
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3110803
Supporting Variants
Samplessample169
Known GenesZNF25
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14088487
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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