A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv980185



Internal ID18268699
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:17910925..17912888hg38UCSC Ensembl
Innerchr4:17912548..17914511hg19UCSC Ensembl
Innerchr4:17521646..17523609hg18UCSC Ensembl
Cytoband4p15.31
Allele length
AssemblyAllele length
hg381964
hg191964
hg181964
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2315107, nssv2315102, nssv2315105, nssv2315108, nssv2315110, nssv2315101, nssv2315104, nssv2315103, nssv2315109, nssv2315106
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesLCORL
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv980185
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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