A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3202660



Internal ID22351789
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:136127023..136264873hg38UCSC Ensembl
chr4:137048178..137186028hg19UCSC Ensembl
Cytoband4q28.3
Allele length
AssemblyAllele length
hg38137851
hg19137851
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6859n152
Supporting Variantsnssv14435172
SamplesHG00514
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3202660
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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