A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv972408



Internal ID18260938
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:83968353..83969898hg38UCSC Ensembl
Innerchr9:86583268..86584813hg19UCSC Ensembl
Innerchr9:85773088..85774633hg18UCSC Ensembl
Cytoband9q21.32
Allele length
AssemblyAllele length
hg381546
hg191546
hg181546
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2555908, nssv2555912, nssv2555904, nssv2555909, nssv2555910, nssv2555907, nssv2555911, nssv2555903, nssv2555906, nssv2555905
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesHNRNPK, MIR7-1
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv972408
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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