A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3959954



Internal ID19222342
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr18:15375301..15410801hg38UCSC Ensembl
Outerchr18:15375300..15410800hg19UCSC Ensembl
Cytoband18p11.1
Allele length
AssemblyAllele length
hg3835501
hg1935501
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1110308
Supporting Variants
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3959954
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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