A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv948108



Internal ID18594954
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:84555724..84570473hg38UCSC Ensembl
Innerchr10:86315480..86330229hg19UCSC Ensembl
Innerchr10:86305460..86320209hg18UCSC Ensembl
Cytoband10q23.1
Allele length
AssemblyAllele length
hg3814750
hg1914750
hg1814750
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1860029, nssv1860030, nssv1860025, nssv1860027, nssv1860021, nssv1860024, nssv1860023, nssv1860026, nssv1860022, nssv1860028
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)nsv948108
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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