A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv968731



Internal ID18257273
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:93564348..93565557hg38UCSC Ensembl
Innerchr9:96326630..96327839hg19UCSC Ensembl
Innerchr9:95366451..95367660hg18UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg381210
hg191210
hg181210
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2560911, nssv2560904, nssv2560910, nssv2560905, nssv2560912, nssv2560913, nssv2560908, nssv2560909, nssv2560907, nssv2560906
SamplesHGDP00927, HGDP00778, HGDP00542, HGDP01029, HGDP01284, HGDP00521, HGDP00998, HGDP00456, HGDP01307, HGDP00665
Known GenesFAM120A
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv968731
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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