A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv947801



Internal ID18247962
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:29507428..29508717hg38UCSC Ensembl
Innerchr10:29796357..29797646hg19UCSC Ensembl
Innerchr10:29836363..29837652hg18UCSC Ensembl
Cytoband10p11.23
Allele length
AssemblyAllele length
hg381290
hg191290
hg181290
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1839017, nssv1839015, nssv1839011, nssv1839018, nssv1839009, nssv1839010, nssv1839013, nssv1839014, nssv1839012, nssv1839016
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesSVIL
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv947801
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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