A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1115518



Internal ID19249689
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr17:26936074..27010574hg38UCSC Ensembl
Outerchr17:25263100..25337600hg19UCSC Ensembl
Cytoband17q11.1
Allele length
AssemblyAllele length
hg3874501
hg1974501
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1449n106
Supporting Variantsnssv3977327
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1115518
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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