A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv982269



Internal ID18617464
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:62483055..62498723hg38UCSC Ensembl
Innerchr9:46794356..46810024hg19UCSC Ensembl
Innerchr9:46634352..46650020hg18UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg3815669
hg1915669
hg1815669
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2543769, nssv2543768, nssv2543765, nssv2543771, nssv2543764, nssv2543770, nssv2543767, nssv2543773, nssv2543766, nssv2543772
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)nsv982269
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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