A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1118474



Internal ID18914464
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:46636117..46642917hg38UCSC Ensembl
Outerchr10:46906700..46913500hg19UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg386801
hg196801
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3958982
SamplesKWS1
Known GenesFAM35BP
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1118474
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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