A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv972771



Internal ID18607987
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:86374821..86386902hg38UCSC Ensembl
Innerchr9:88989736..89001817hg19UCSC Ensembl
Innerchr9:88179556..88191637hg18UCSC Ensembl
Cytoband9q21.33
Allele length
AssemblyAllele length
hg3812082
hg1912082
hg1812082
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2555770, nssv2555765, nssv2555768, nssv2555769, nssv2555767, nssv2555764, nssv2555766, nssv2555762, nssv2555763, nssv2555771
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)nsv972771
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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