A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv982349



Internal ID18270858
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:130489116..130496766hg38UCSC Ensembl
Innerchr9:133364503..133372153hg19UCSC Ensembl
Innerchr9:132354324..132361974hg18UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg387651
hg197651
hg187651
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2567091, nssv2567092, nssv2567097, nssv2567100, nssv2567096, nssv2567094, nssv2567093, nssv2567095, nssv2567099, nssv2567098
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)nsv982349
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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