A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2027728



Internal ID17748584
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:62953154..62956435hg38UCSC Ensembl
Innerchr15:63245353..63248634hg19UCSC Ensembl
Innerchr15:61032406..61035687hg18UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg383282
hg193282
hg183282
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv977728
Supporting Variants
SamplesHGDP00521
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)nssv2027728
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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