A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3764144



Internal ID19313537
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:64359030..64369408hg38UCSC Ensembl
chr9:43133699..43144100hg19UCSC Ensembl
Cytoband9p12
Allele length
AssemblyAllele length
hg3810379
hg1910402
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1078061
Supporting Variants
SamplesKWP1
Known GenesLOC642929
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3764144
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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