A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2528898



Internal ID17786913
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 StatusS
Merged Variantsnsv982218
Supporting Variants
SamplesHGDP00665
Known GenesANKRD18A, FAM201A, FAM95C
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Commentslineage specific duplication - fixed_Pab-Ppy-Ggod-Ggog-Gbeg-Ptrs-Ptrt-Ptre-Ptrv-Ppa-Hsa-Hde
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nssv2528898
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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