A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2552290



Internal ID17404827
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:65659539..65670621hg38UCSC Ensembl
Innerchr9:70495424..70506535hg19UCSC Ensembl
Innerchr9:69735244..69746489hg18UCSC Ensembl
Cytoband9q12
Allele length
AssemblyAllele length
hg3811083
hg1911112
hg1811246
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv972396
Supporting Variants
SamplesHGDP00521
Known Genes
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Commentslineage specific duplication - fixed_Hsa-Hde
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nssv2552290
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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