A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1079002



Internal ID19320691
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:158886209..158892110hg38UCSC Ensembl
chr1:158855999..158861900hg19UCSC Ensembl
Cytoband1q23.1
Allele length
AssemblyAllele length
hg385902
hg195902
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3764643
SamplesKWP1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1079002
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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