A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv982281



Internal ID18617476
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:63110185..63202862hg38UCSC Ensembl
Innerchr9:67015157..67107834hg19UCSC Ensembl
Innerchr9:66754977..66847905hg18UCSC Ensembl
Cytoband9q12
Allele length
AssemblyAllele length
hg3892678
hg1992678
hg1892929
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2548155, nssv2548156, nssv2548159, nssv2548162, nssv2548161, nssv2548157, nssv2548153, nssv2548160, nssv2548154, nssv2548158
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesLOC286297
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv982281
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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