A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3988854



Internal ID18879758
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 StatusS
Merged Variantsnsv1135296
Supporting Variants
SamplesKWS2
Known GenesKIAA1958
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3988854
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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