A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv948127



Internal ID18594973
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:87642279..87643868hg38UCSC Ensembl
Innerchr10:89402036..89403625hg19UCSC Ensembl
Innerchr10:89392016..89393605hg18UCSC Ensembl
Cytoband10q23.2
Allele length
AssemblyAllele length
hg381590
hg191590
hg181590
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1861676, nssv1861673, nssv1861682, nssv1861679, nssv1861678, nssv1861681, nssv1861677, nssv1861675, nssv1861680, nssv1861674
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)nsv948127
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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