A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv948183



Internal ID18595029
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:110448221..110455403hg38UCSC Ensembl
Innerchr10:112207979..112215161hg19UCSC Ensembl
Innerchr10:112197969..112205151hg18UCSC Ensembl
Cytoband10q25.2
Allele length
AssemblyAllele length
hg387183
hg197183
hg187183
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1867885, nssv1867887, nssv1867890, nssv1867881, nssv1867889, nssv1867886, nssv1867888, nssv1867884, nssv1867882, nssv1867883
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)nsv948183
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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