A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv982258



Internal ID18270767
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:61862957..61910760hg38UCSC Ensembl
Innerchr9:44999109..45046912hg19UCSC Ensembl
Innerchr9:44939105..44986908hg18UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg3847804
hg1947804
hg1847804
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2541236, nssv2541237, nssv2541231, nssv2541235, nssv2541233, nssv2541238, nssv2541234, nssv2541230, nssv2541239, nssv2541232
SamplesHGDP00927, HGDP00778, HGDP00542, HGDP01029, HGDP01284, HGDP00521, HGDP00998, HGDP00456, HGDP01307, HGDP00665
Known Genes
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv982258
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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