A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3981327



Internal ID19211456
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:60591301..60592601hg38UCSC Ensembl
Outerchr15:60883500..60884800hg19UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg381301
hg191301
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1144737
Supporting Variants
SamplesKWS1
Known GenesRORA
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3981327
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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