A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv968730



Internal ID18257272
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:93514566..93516279hg38UCSC Ensembl
Innerchr9:96276848..96278561hg19UCSC Ensembl
Innerchr9:95316669..95318382hg18UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg381714
hg191714
hg181714
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2560811, nssv2560812, nssv2560813, nssv2560816, nssv2560808, nssv2560809, nssv2560815, nssv2560814, nssv2560810, nssv2560807
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesFAM120A
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv968730
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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