A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3764678



Internal ID18964135
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:55754638..55761639hg38UCSC Ensembl
chr17:53831999..53839000hg19UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg387002
hg197002
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1076450
Supporting Variants
SamplesKWP1
Known GenesPCTP
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3764678
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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