A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2729419



Internal ID17784175
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:40263761..40269664hg38UCSC Ensembl
Innerchr9:42408779..42414682hg19UCSC Ensembl
Innerchr9:42398775..42404678hg18UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg385904
hg195904
hg185904
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv982402
Supporting Variants
SamplesHGDP00665
Known GenesANKRD20A2, ANKRD20A3
MethodSequencing
Analysislineage specific fixed expansions
PlatformNot reported
Commentslineage specific expansions - expansion_Ggod-Ggog-Gbeg-Ptrs-Ptrt-Ptre-Ptrv-Ppa-Hsa-Hde
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nssv2729419
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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