A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1134669



Internal ID19285062
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr17:68231415..68231636hg38UCSC Ensembl
Outerchr17:66227556..66227777hg19UCSC Ensembl
Cytoband17q24.2
Allele length
AssemblyAllele length
hg38222
hg19222
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1500n106
Supporting Variantsnssv3989217, nssv3972118
SamplesKWS2, KWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1134669
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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