A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3978830



Internal ID18887403
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:131919654..131919719hg38UCSC Ensembl
Outerchr10:133733158..133733223hg19UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1140118
Supporting Variants
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3978830
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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