A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2998060



Internal ID16944326
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:118595189..118596388hg38UCSC Ensembl
Outerchr10:120354701..120355900hg19UCSC Ensembl
Cytoband10q26.11
Allele length
AssemblyAllele length
hg381200
hg191200
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv951861
Supporting Variants
SamplesBILGI_BIOE
Known GenesPRLHR
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv2998060
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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