A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv975380



Internal ID18610588
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:76010631..76017178hg38UCSC Ensembl
Innerchr11:75721675..75728222hg19UCSC Ensembl
Innerchr11:75399323..75405870hg18UCSC Ensembl
Cytoband11q13.5
Allele length
AssemblyAllele length
hg386548
hg196548
hg186548
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2763407
SamplesHGDP00998
Known GenesUVRAG
MethodSequencing
AnalysisHuman CNVs
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv975380
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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