A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv948182



Internal ID18248342
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:110253779..110258102hg38UCSC Ensembl
Innerchr10:112013537..112017860hg19UCSC Ensembl
Innerchr10:112003527..112007850hg18UCSC Ensembl
Cytoband10q25.2
Allele length
AssemblyAllele length
hg384324
hg194324
hg184324
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1867792, nssv1867789, nssv1867791, nssv1867785, nssv1867788, nssv1867793, nssv1867784, nssv1867787, nssv1867786, nssv1867790
SamplesHGDP00927, HGDP00778, HGDP00542, HGDP01029, HGDP01284, HGDP00521, HGDP00998, HGDP00456, HGDP01307, HGDP00665
Known GenesMXI1
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv948182
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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