A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv982218



Internal ID18617413
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:38524397..38630634hg38UCSC Ensembl
Innerchr9:38524394..38630631hg19UCSC Ensembl
Innerchr9:38514394..38620631hg18UCSC Ensembl
Cytoband9p13.1
Allele length
AssemblyAllele length
hg38106238
hg19106238
hg18106238
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2528891, nssv2528892, nssv2528894, nssv2528896, nssv2528890, nssv2528895, nssv2528899, nssv2528893, nssv2528898, nssv2528897
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesANKRD18A, FAM201A, FAM95C
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv982218
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer