A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv982310



Internal ID18617505
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:79389889..79393537hg38UCSC Ensembl
Innerchr9:82004804..82008452hg19UCSC Ensembl
Innerchr9:81194624..81198272hg18UCSC Ensembl
Cytoband9q21.31
Allele length
AssemblyAllele length
hg383649
hg193649
hg183649
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2553594, nssv2553600, nssv2553593, nssv2553592, nssv2553595, nssv2553591, nssv2553596, nssv2553599, nssv2553598, nssv2553597
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)nsv982310
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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