A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1078065



Internal ID19324147
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:40657433..40679750hg38UCSC Ensembl
chr11:40678983..40701300hg19UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg3822318
hg1922318
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3763801
SamplesKWP1
Known GenesLRRC4C
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1078065
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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