A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1118765



Internal ID18907742
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr17:49361838..49362438hg38UCSC Ensembl
Outerchr17:47439200..47439800hg19UCSC Ensembl
Cytoband17q21.33
Allele length
AssemblyAllele length
hg38601
hg19601
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3981075
SamplesKWS1
Known GenesZNF652
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1118765
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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