A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1070836



Internal ID19316177
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:57955038..57955439hg38UCSC Ensembl
chr17:56032399..56032800hg19UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg38402
hg19402
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3772323
SamplesKWP1
Known GenesCUEDC1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1070836
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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