A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1075607



Internal ID19315801
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:15445576..15445636hg38UCSC Ensembl
chr9:15445574..15445634hg19UCSC Ensembl
Cytoband9p22.3
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3771258
SamplesKWP1
Known GenesSNAPC3
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1075607
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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