A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1069607



Internal ID18974462
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:72092858..72095859hg38UCSC Ensembl
chr15:72385199..72388200hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg383002
hg193002
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3761963
SamplesKWP1
Known GenesMYO9A
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1069607
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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