A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3762296



Internal ID18958702
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:8829285..8829369hg38UCSC Ensembl
chr17:8732602..8732686hg19UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg3885
hg1985
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1071370
Supporting Variants
SamplesKWP1
Known GenesPIK3R6
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3762296
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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