A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14090140



Internal ID21268615
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:95742285..95780356hg38UCSC Ensembl
Innerchr10:97502042..97540113hg19UCSC Ensembl
Cytoband10q24.1
Allele length
AssemblyAllele length
hg3838072
hg1938072
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3113375
Supporting Variants
Samplessample128
Known GenesENTPD1, ENTPD1-AS1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14090140
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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