A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv948184



Internal ID18595030
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:110547193..110550290hg38UCSC Ensembl
Innerchr10:112306951..112310048hg19UCSC Ensembl
Innerchr10:112296941..112300038hg18UCSC Ensembl
Cytoband10q25.2
Allele length
AssemblyAllele length
hg383098
hg193098
hg183098
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1867979, nssv1867982, nssv1867985, nssv1867984, nssv1867986, nssv1867983, nssv1867981, nssv1867978, nssv1867980, nssv1867987
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)nsv948184
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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