A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv982334



Internal ID18270843
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:105520481..105527183hg38UCSC Ensembl
Innerchr9:108282762..108289464hg19UCSC Ensembl
Innerchr9:107322583..107329285hg18UCSC Ensembl
Cytoband9q31.2
Allele length
AssemblyAllele length
hg386703
hg196703
hg186703
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2563152, nssv2563161, nssv2563157, nssv2563160, nssv2563153, nssv2563155, nssv2563159, nssv2563156, nssv2563154, nssv2563158
SamplesHGDP00927, HGDP00778, HGDP00542, HGDP01029, HGDP01284, HGDP00521, HGDP00998, HGDP00456, HGDP01307, HGDP00665
Known GenesFSD1L
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv982334
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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