A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv947902



Internal ID18594749
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:45055188..45059370hg38UCSC Ensembl
Innerchr10:45550636..45554818hg19UCSC Ensembl
Innerchr10:44870642..44874824hg18UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg384183
hg194183
hg184183
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1844635, nssv1844642, nssv1844637, nssv1844643, nssv1844638, nssv1844641, nssv1844636, nssv1844639, nssv1844640, nssv1844644
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known Genes
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv947902
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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