A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3770736



Internal ID19313702
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:33691780..33698281hg38UCSC Ensembl
chr17:32018799..32025300hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg386502
hg196502
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1076447
Supporting Variants
SamplesKWP1
Known GenesASIC2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3770736
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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