A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv982242



Internal ID18617437
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:40202473..40219542hg38UCSC Ensembl
Innerchr9:42347491..42364560hg19UCSC Ensembl
Innerchr9:42337487..42354556hg18UCSC Ensembl
Cytoband9p12
Allele length
AssemblyAllele length
hg3817070
hg1917070
hg1817070
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2535383, nssv2535387, nssv2535385, nssv2535390, nssv2535388, nssv2535386, nssv2535381, nssv2535389, nssv2535384, nssv2535382
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)nsv982242
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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