A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv982336



Internal ID18617531
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:107456204..107458972hg38UCSC Ensembl
Innerchr9:110218485..110221253hg19UCSC Ensembl
Innerchr9:109258306..109261074hg18UCSC Ensembl
Cytoband9q31.2
Allele length
AssemblyAllele length
hg382769
hg192769
hg182769
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2561482, nssv2561484, nssv2561483, nssv2561481, nssv2561485, nssv2561488, nssv2561479, nssv2561486, nssv2561487, nssv2561480
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)nsv982336
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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