A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2733580



Internal ID17840025
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:42896180..42897018hg38UCSC Ensembl
Innerchr9:44074101..44074939hg19UCSC Ensembl
Innerchr9:44014097..44014935hg18UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg38839
hg19839
hg18839
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv969594
Supporting Variants
SamplesHGDP00998
Known Genes
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)nssv2733580
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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