A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1075830



Internal ID18975082
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:34483352..34484553hg38UCSC Ensembl
chr11:34504899..34506100hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg381202
hg191202
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3769246
SamplesKWP1
Known GenesELF5
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1075830
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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