A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv947813



Internal ID18594660
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:30672472..30678086hg38UCSC Ensembl
Innerchr10:30961401..30967015hg19UCSC Ensembl
Innerchr10:31001407..31007021hg18UCSC Ensembl
Cytoband10p11.23
Allele length
AssemblyAllele length
hg385615
hg195615
hg185615
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1838586, nssv1838589, nssv1838591, nssv1838593, nssv1838585, nssv1838588, nssv1838587, nssv1838592, nssv1838590, nssv1838594
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)nsv947813
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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