A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1115233



Internal ID19251724
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:128865037..128865100hg38UCSC Ensembl
Outerchr9:131627316..131627379hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3976287
SamplesKWS2
Known GenesCCBL1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1115233
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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