A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv982508



Internal ID18617703
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:64375278..64382886hg38UCSC Ensembl
Innerchr9:69387696..69395304hg19UCSC Ensembl
Innerchr9:68677516..68685124hg18UCSC Ensembl
Cytoband9q12
Allele length
AssemblyAllele length
hg387609
hg197609
hg187609
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2743542, nssv2743538, nssv2743539, nssv2743543, nssv2743537, nssv2743540, nssv2743536, nssv2743535, nssv2743541, nssv2743534
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesANKRD20A4
MethodSequencing
Analysislineage specific fixed expansions
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv982508
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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