A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3977850



Internal ID19241690
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:62798876..62888276hg38UCSC Ensembl
Outerchr9:66454700..66544100hg19UCSC Ensembl
Cytoband9q13
Allele length
AssemblyAllele length
hg3889401
hg1989401
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1139973
Supporting Variants
SamplesKWS2
Known GenesPTGER4P2-CDK2AP2P2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3977850
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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