A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3989215



Internal ID18870598
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr17:67731238..67731514hg38UCSC Ensembl
Outerchr17:65727354..65727630hg19UCSC Ensembl
Cytoband17q24.2
Allele length
AssemblyAllele length
hg38277
hg19277
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1135506
Supporting Variants
SamplesKWS1
Known GenesNOL11
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3989215
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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