A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1077328



Internal ID19326635
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:176599..195700hg38UCSC Ensembl
chr11:176599..195700hg19UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg3819102
hg1919102
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3764558
SamplesKWP1
Known GenesLOC653486, SCGB1C1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1077328
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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