A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2998082



Internal ID16944348
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:132093297..132212896hg38UCSC Ensembl
Outerchr10:133906801..134026400hg19UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg38119600
hg19119600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv951885
Supporting Variants
SamplesBILGI_BIOE
Known GenesDPYSL4, JAKMIP3, STK32C
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv2998082
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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