A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv972651



Internal ID18607867
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:14203792..14205782hg38UCSC Ensembl
Innerchr9:14203791..14205781hg19UCSC Ensembl
Innerchr9:14193791..14195781hg18UCSC Ensembl
Cytoband9p22.3
Allele length
AssemblyAllele length
hg381991
hg191991
hg181991
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2523069, nssv2523065, nssv2523066, nssv2523060, nssv2523067, nssv2523068, nssv2523061, nssv2523062, nssv2523063, nssv2523064
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesNFIB
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv972651
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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