A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3199351



Internal ID22348947
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:155196633..155214572hg38UCSC Ensembl
Outerchr4:156117785..156135724hg19UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg3817940
hg1917940
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14272779
SamplesHG00514
Known GenesNPY2R
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3199351
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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