A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3990130



Internal ID18879484
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:14313801..14316701hg38UCSC Ensembl
Outerchr9:14313800..14316700hg19UCSC Ensembl
Cytoband9p22.3
Allele length
AssemblyAllele length
hg382901
hg192901
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1137629
Supporting Variants
SamplesKWS2
Known GenesNFIB
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3990130
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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