A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2161771



Internal ID17516738
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:3576184..3576684hg38UCSC Ensembl
Innerchr2:3623774..3624274hg19UCSC Ensembl
Innerchr2:3601649..3602149hg18UCSC Ensembl
Cytoband2p25.3
Allele length
AssemblyAllele length
hg38501
hg19501
hg18501
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv978973
Supporting Variants
SamplesHGDP01284
Known GenesRPS7
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)nssv2161771
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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