A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3978927



Internal ID19226658
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:4735316..4735376hg38UCSC Ensembl
Outerchr9:4735316..4735376hg19UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1140215
Supporting Variants
SamplesKWS2
Known GenesAK3
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3978927
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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