A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1070950



Internal ID18973485
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:35943449..35944450hg38UCSC Ensembl
chr11:35964999..35966000hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg381002
hg191002
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3770019
SamplesKWP1
Known GenesLDLRAD3
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1070950
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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