A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv948195



Internal ID18595041
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:116438609..116440376hg38UCSC Ensembl
Innerchr10:118198121..118199888hg19UCSC Ensembl
Innerchr10:118188111..118189878hg18UCSC Ensembl
Cytoband10q25.3
Allele length
AssemblyAllele length
hg381768
hg191768
hg181768
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1868116, nssv1868112, nssv1868119, nssv1868118, nssv1868110, nssv1868115, nssv1868113, nssv1868117, nssv1868111, nssv1868114
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesPNLIPRP3
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv948195
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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