A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3768659



Internal ID19312860
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:34987702..34991803hg38UCSC Ensembl
chr9:34987699..34991800hg19UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg384102
hg194102
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1077101
Supporting Variants
SamplesKWP1
Known GenesDNAJB5, LOC101926900
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3768659
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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