A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv972455



Internal ID18260985
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:130458369..130459908hg38UCSC Ensembl
Innerchr9:133333756..133335295hg19UCSC Ensembl
Innerchr9:132323577..132325116hg18UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg381540
hg191540
hg181540
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2566996, nssv2566994, nssv2566998, nssv2567002, nssv2566999, nssv2567001, nssv2566997, nssv2566995, nssv2567000, nssv2567003
SamplesHGDP00927, HGDP00778, HGDP00542, HGDP01029, HGDP01284, HGDP00521, HGDP00998, HGDP00456, HGDP01307, HGDP00665
Known GenesASS1
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv972455
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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