A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2532382



Internal ID17809317
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:39412910..39440246hg38UCSC Ensembl
Innerchr9:39412907..39440245hg19UCSC Ensembl
Innerchr9:39402907..39430245hg18UCSC Ensembl
Cytoband9p13.1
Allele length
AssemblyAllele length
hg3827337
hg1927339
hg1827339
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv968622
Supporting Variants
SamplesHGDP00778
Known Genes
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)nssv2532382
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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