A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv972402



Internal ID18260932
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:76397805..76400577hg38UCSC Ensembl
Innerchr9:79012721..79015493hg19UCSC Ensembl
Innerchr9:78202541..78205313hg18UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg382773
hg192773
hg182773
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2554376, nssv2554374, nssv2554380, nssv2553579, nssv2554379, nssv2554378, nssv2554377, nssv2554375, nssv2554373, nssv2554372
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesRPSAP9
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv972402
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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