A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2752008



Internal ID17851575
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:65830543..65846000hg38UCSC Ensembl
Innerchr9:70318730..70335502hg19UCSC Ensembl
Innerchr9:69558373..69575322hg18UCSC Ensembl
Cytoband9q12
Allele length
AssemblyAllele length
hg3815458
hg1916773
hg1816950
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv982297
Supporting Variants
SamplesHGDP01029
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)nssv2752008
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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