A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3975745



Internal ID18891479
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:92380480..92380549hg38UCSC Ensembl
Outerchr9:95142762..95142831hg19UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg3870
hg1970
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1124448
Supporting Variants
SamplesKWS2
Known GenesCENPP
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3975745
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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