A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3771155



Internal ID19313486
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:54526080..54552081hg38UCSC Ensembl
chr11:51567199..51593200hg19UCSC Ensembl
Cytoband11p11.12
Allele length
AssemblyAllele length
hg3826002
hg1926002
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1075834
Supporting Variants
SamplesKWP1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3771155
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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