A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv972369



Internal ID18607585
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:62498723..62521809hg38UCSC Ensembl
Innerchr9:46810024..46833110hg19UCSC Ensembl
Innerchr9:46650020..46673106hg18UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg3823087
hg1923087
hg1823087
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv91n82
Supporting Variantsnssv2544636, nssv2544641, nssv2544637, nssv2544638, nssv2544643, nssv2544640, nssv2544644, nssv2544645, nssv2544642, nssv2544639
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesLOC643648
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv972369
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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