A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2999127



Internal ID16945393
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:70043962..70061561hg38UCSC Ensembl
Outerchr15:70336301..70353900hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg3817600
hg1917600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv951987
Supporting Variants
SamplesBILGI_BIOE
Known GenesTLE3
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv2999127
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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