A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3958858



Internal ID18861170
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:128525740..128525806hg38UCSC Ensembl
Outerchr9:131288019..131288085hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg3867
hg1967
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1118369
Supporting Variants
SamplesKWS1
Known GenesGLE1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3958858
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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