A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2287897



Internal ID17782260
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:93931605..93932105hg38UCSC Ensembl
Innerchr3:93650449..93650949hg19UCSC Ensembl
Innerchr3:95133139..95133639hg18UCSC Ensembl
Cytoband3q11.1
Allele length
AssemblyAllele length
hg38501
hg19501
hg18501
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv965187
Supporting Variants
SamplesHGDP00665
Known GenesPROS1
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Commentslineage specific duplication - fixed_Ggod-Ggog-Gbeg-Ptrs-Ptrt-Ptre-Ptrv-Ppa-Hsa-Hde
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nssv2287897
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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