A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1111118



Internal ID18905001
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:71975323..71975412hg38UCSC Ensembl
Outerchr15:72267664..72267753hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg3890
hg1990
Variant TypeCNV tandem duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3962341
SamplesKWS1
Known GenesMYO9A
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1111118
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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