A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1138372



Internal ID19285198
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:52341670..52341769hg38UCSC Ensembl
Outerchr15:52633867..52633966hg19UCSC Ensembl
Cytoband15q21.2
Allele length
AssemblyAllele length
hg38100
hg19100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3990934
SamplesKWS2
Known GenesMYO5A
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1138372
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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