A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1134637



Internal ID19256886
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr17:31070566..31070616hg38UCSC Ensembl
Outerchr17:29397584..29397634hg19UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg3851
hg1951
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1454n106
Supporting Variantsnssv3972514
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1134637
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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