A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1070992



Internal ID19316377
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:118875586..118875735hg38UCSC Ensembl
chr11:118746295..118746444hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg38150
hg19150
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3766569
SamplesKWP1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1070992
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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