A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3984345



Internal ID18874876
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:72093660..72095811hg38UCSC Ensembl
Outerchr15:72386001..72388152hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg382152
hg192152
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1126137
Supporting Variants
SamplesKWS1
Known GenesMYO9A
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3984345
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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