A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv972393



Internal ID18607609
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:65166952..65169800hg38UCSC Ensembl
Innerchr9:70060552..70063406hg19UCSC Ensembl
Innerchr9:69350372..69353226hg18UCSC Ensembl
Cytoband9q12
Allele length
AssemblyAllele length
hg382849
hg192855
hg182855
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2753955, nssv2746927, nssv2752827, nssv2749226, nssv2748294, nssv2750520, nssv2756127, nssv2750069, nssv2754364, nssv2751128, nssv2749834, nssv2749594, nssv2753375, nssv2747393, nssv2754169, nssv2750373, nssv2756238, nssv2755637, nssv2752899, nssv2750793
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known Genes
MethodSequencing
Analysislineage specific fixed expansions
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv972393
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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