A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2528795



Internal ID17875406
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:36299954..36314407hg38UCSC Ensembl
Innerchr9:36299951..36314404hg19UCSC Ensembl
Innerchr9:36289951..36304404hg18UCSC Ensembl
Cytoband9p13.2
Allele length
AssemblyAllele length
hg3814454
hg1914454
hg1814454
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv972312
Supporting Variants
SamplesHGDP01284
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)nssv2528795
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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