A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3765359



Internal ID18962198
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:11240382..11241583hg38UCSC Ensembl
chr17:11143699..11144900hg19UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg381202
hg191202
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1070809
Supporting Variants
SamplesKWP1
Known GenesSHISA6
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3765359
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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