A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv972706



Internal ID18607922
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:65270665..65282593hg38UCSC Ensembl
Innerchr9:42719850..42731774hg19UCSC Ensembl
Innerchr9:42709846..42721770hg18UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg3811929
hg1911925
hg1811925
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2536684, nssv2536683, nssv2536685, nssv2536689, nssv2536681, nssv2536682, nssv2536680, nssv2536688, nssv2536686, nssv2536687
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesFOXD4L2, FOXD4L4
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv972706
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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