A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3959287



Internal ID18858307
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:112665036..112665086hg38UCSC Ensembl
Outerchr9:115427316..115427366hg19UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg3851
hg1951
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1110053
Supporting Variants
SamplesKWS1
Known GenesKIAA1958
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3959287
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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