A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4011955



Internal ID22073586
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:50350980..50439635hg38UCSC Ensembl
Outerchr18:50341374..50442864hg38UCSC Ensembl
Innerchr18:47877350..47966005hg19UCSC Ensembl
Outerchr18:47867744..47969234hg19UCSC Ensembl
Cytoband18q21.1
Allele length
AssemblyAllele length
hg38101491
hg19101491
Variant TypeCNV duplication
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1155515
Supporting Variants
Samples
Known GenesSKA1
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4011955
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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