A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2999125



Internal ID17292077
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:69382062..69396861hg38UCSC Ensembl
Outerchr15:69674401..69689200hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg3814800
hg1914800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv951985
Supporting Variants
SamplesBILGI_BIOE
Known GenesPAQR5
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv2999125
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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