A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3201534



Internal ID22350827
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:156180523..156180890hg38UCSC Ensembl
chr1:156150314..156150681hg19UCSC Ensembl
Cytoband1q22
Allele length
AssemblyAllele length
hg38368
hg19368
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv431n152
Supporting Variantsnssv14405056
SamplesNA19240
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3201534
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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