A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv948110



Internal ID18594956
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:86630093..86632568hg38UCSC Ensembl
Innerchr10:88389850..88392325hg19UCSC Ensembl
Innerchr10:88379830..88382305hg18UCSC Ensembl
Cytoband10q23.2
Allele length
AssemblyAllele length
hg382476
hg192476
hg182476
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1861008, nssv1861013, nssv1861009, nssv1861010, nssv1861005, nssv1861011, nssv1861006, nssv1861014, nssv1861012, nssv1861007
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)nsv948110
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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