A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1112506



Internal ID19275048
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:17899520..17902885hg38UCSC Ensembl
Outerchr9:17899518..17902883hg19UCSC Ensembl
Cytoband9p22.2
Allele length
AssemblyAllele length
hg383366
hg193366
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3989655, nssv3994227
SamplesKWS2, KWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1112506
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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