A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1079029



Internal ID19322617
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:166247962..166248863hg38UCSC Ensembl
chr1:166217199..166218100hg19UCSC Ensembl
Cytoband1q24.1
Allele length
AssemblyAllele length
hg38902
hg19902
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3766982
SamplesKWP1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1079029
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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