A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3962397



Internal ID18869737
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr18:11874556..11880210hg38UCSC Ensembl
Outerchr18:11874555..11880209hg19UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg385655
hg195655
Variant TypeCNV tandem duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1111154
Supporting Variants
SamplesKWS1
Known GenesGNAL
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3962397
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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