A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv972801



Internal ID18261331
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:112496667..112498047hg38UCSC Ensembl
Innerchr9:115258947..115260327hg19UCSC Ensembl
Innerchr9:114298768..114300148hg18UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg381381
hg191381
hg181381
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2565622, nssv2565620, nssv2565625, nssv2565628, nssv2565623, nssv2565621, nssv2565626, nssv2565624, nssv2565619, nssv2565627
SamplesHGDP00927, HGDP00778, HGDP00542, HGDP01029, HGDP01284, HGDP00521, HGDP00998, HGDP00456, HGDP01307, HGDP00665
Known GenesKIAA1958
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv972801
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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