A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv947932



Internal ID18248092
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46375720..46397324hg38UCSC Ensembl
Innerchr10:47152438..47174050hg19UCSC Ensembl
Innerchr10:46572444..46594056hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg3821605
hg1921613
hg1821613
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1844875, nssv1844876, nssv1844867, nssv1844871, nssv1844868, nssv1844870, nssv1844874, nssv1844869, nssv1844872, nssv1844873
SamplesHGDP00927, HGDP00778, HGDP00542, HGDP01029, HGDP01284, HGDP00521, HGDP00998, HGDP00456, HGDP01307, HGDP00665
Known GenesANXA8
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv947932
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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