A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv947734



Internal ID18594581
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:8514103..8515549hg38UCSC Ensembl
Innerchr10:8556066..8557512hg19UCSC Ensembl
Innerchr10:8596072..8597518hg18UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg381447
hg191447
hg181447
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1833012, nssv1833018, nssv1833011, nssv1833010, nssv1833013, nssv1833009, nssv1833017, nssv1833016, nssv1833015, nssv1833014
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)nsv947734
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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