A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1070069



Internal ID18977442
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:113935159..113935459hg38UCSC Ensembl
chr11:113805881..113806181hg19UCSC Ensembl
Cytoband11q23.2
Allele length
AssemblyAllele length
hg38301
hg19301
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3765096
SamplesKWP1
Known GenesHTR3B
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1070069
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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