A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3770362



Internal ID18964496
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:17325202..17325285hg38UCSC Ensembl
chr9:17325200..17325283hg19UCSC Ensembl
Cytoband9p22.2
Allele length
AssemblyAllele length
hg3884
hg1984
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1077094
Supporting Variants
SamplesKWP1
Known GenesCNTLN
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3770362
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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