A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv948222



Internal ID18595068
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:125272076..125272576hg38UCSC Ensembl
Innerchr10:126960645..126961145hg19UCSC Ensembl
Innerchr10:126950635..126951135hg18UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg38501
hg19501
hg18501
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1870616, nssv1870624, nssv1870619, nssv1870615, nssv1870618, nssv1870621, nssv1870623, nssv1870620, nssv1870622, nssv1870617
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)nsv948222
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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