A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv947838



Internal ID18594685
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:36522258..36522966hg38UCSC Ensembl
Innerchr10:36811186..36811894hg19UCSC Ensembl
Innerchr10:36851192..36851900hg18UCSC Ensembl
Cytoband10p11.21
Allele length
AssemblyAllele length
hg38709
hg19709
hg18709
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1839739, nssv1839745, nssv1839736, nssv1839744, nssv1839740, nssv1839737, nssv1839738, nssv1839743, nssv1839741, nssv1839742
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)nsv947838
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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