A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3987677



Internal ID18869777
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr18:79684890..79684972hg38UCSC Ensembl
Outerchr18:77444890..77444972hg19UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg3883
hg1983
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1132883
Supporting Variants
SamplesKWS1
Known GenesCTDP1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3987677
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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