A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6197n152



Internal ID22821900
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:150821830..150821926hg38UCSC Ensembl
chr3:150539617..150539713hg19UCSC Ensembl
Cytoband3q25.1
Allele length
AssemblyAllele length
hg3897
hg1997
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3281841, nsv3283012
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)dgv6197n152
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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