A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv972292



Internal ID18260822
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:3364349..3365736hg38UCSC Ensembl
Innerchr9:3364349..3365736hg19UCSC Ensembl
Innerchr9:3354349..3355736hg18UCSC Ensembl
Cytoband9p24.2
Allele length
AssemblyAllele length
hg381388
hg191388
hg181388
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2520477, nssv2520478, nssv2520475, nssv2520476, nssv2520474, nssv2520472, nssv2520470, nssv2520479, nssv2520471, nssv2520473
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesRFX3
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv972292
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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