A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3955110



Internal ID19216239
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:22868570..22868622hg38UCSC Ensembl
Outerchr15:23004446..23004498hg19UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1127416
Supporting Variants
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3955110
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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