A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1134584



Internal ID19280014
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr17:974243..974308hg38UCSC Ensembl
Outerchr17:877483..877548hg19UCSC Ensembl
Cytoband17p13.3
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3972466
SamplesKWS2
Known GenesNXN
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1134584
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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