A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3201766



Internal ID22351021
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:41883099..41884793hg38UCSC Ensembl
chr1:42348770..42350464hg19UCSC Ensembl
Cytoband1p34.2
Allele length
AssemblyAllele length
hg381695
hg191695
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14363133
SamplesHG00512
Known GenesHIVEP3
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3201766
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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