A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv982348



Internal ID18270857
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:130453825..130455860hg38UCSC Ensembl
Innerchr9:133329212..133331247hg19UCSC Ensembl
Innerchr9:132319033..132321068hg18UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg382036
hg192036
hg182036
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2568739, nssv2568742, nssv2568743, nssv2568737, nssv2568740, nssv2568744, nssv2568746, nssv2568738, nssv2568745, nssv2568741
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)nsv982348
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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