A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1135296



Internal ID18921049
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:112502336..112502474hg38UCSC Ensembl
Outerchr9:115264616..115264754hg19UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg38139
hg19139
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3988854
SamplesKWS2
Known GenesKIAA1958
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1135296
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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