A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv972946



Internal ID18261476
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:10501600..10513438hg38UCSC Ensembl
Innerchr11:10523147..10534985hg19UCSC Ensembl
Innerchr11:10479723..10491561hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3811839
hg1911839
hg1811839
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2763831, nssv2759313, nssv2762286
SamplesHGDP00778, HGDP01029, HGDP00998
Known GenesAMPD3, MIR4485, MTRNR2L8, RNF141
MethodSequencing
AnalysisHuman CNVs
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv972946
Frequency
Sample Size10
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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