A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6555n152



Internal ID22822258
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:37036685..37036846hg38UCSC Ensembl
chr4:37038307..37038468hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg38162
hg19162
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3280236, nsv3280991
SamplesHG00733, HG00514
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)dgv6555n152
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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