A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv962876



Internal ID18598118
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:39333747..39336035hg38UCSC Ensembl
Innerchr18:36913711..36915999hg19UCSC Ensembl
Innerchr18:35167709..35169997hg18UCSC Ensembl
Cytoband18q12.2
Allele length
AssemblyAllele length
hg382289
hg192289
hg182289
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2121776, nssv2121773, nssv2121775, nssv2121772, nssv2121770, nssv2121768, nssv2121774, nssv2121777, nssv2121771, nssv2121769
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesLINC00669
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv962876
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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