A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv972433



Internal ID18607649
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:97199777..97221161hg38UCSC Ensembl
Innerchr9:99962059..99983443hg19UCSC Ensembl
Innerchr9:99001880..99023264hg18UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg3821385
hg1921385
hg1821385
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2561162, nssv2561168, nssv2561167, nssv2561160, nssv2561159, nssv2561164, nssv2561161, nssv2561165, nssv2561166, nssv2561163
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known Genes
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv972433
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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