A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3978826



Internal ID18884212
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:1159687..1159768hg38UCSC Ensembl
Outerchr10:1205627..1205708hg19UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg3882
hg1982
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1140114
Supporting Variants
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3978826
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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