A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2616657



Internal ID17773753
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:96759..104869hg38UCSC Ensembl
Innerchr11:96759..104869hg19UCSC Ensembl
Innerchr11:86759..94869hg18UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg388111
hg198111
hg188111
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv975136
Supporting Variants
SamplesHGDP00542
Known Genes
MethodSequencing
Analysislineage specific fixed expansions
PlatformNot reported
Commentslineage specific expansions - expansion_Ptrs-Ptrt-Ptre-Ptrv-Ppa-Hsa-Hde
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nssv2616657
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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