A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7861n152



Internal ID22823564
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:38144172..38144224hg38UCSC Ensembl
chr6:38111948..38112000hg19UCSC Ensembl
Cytoband6p21.2
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3527692, nsv3288983
SamplesNA19239, NA19240, HG00514
Known GenesZFAND3
MethodMerging
Sequencing
AnalysisMultiple analysis algorthms
PhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformIllumina HiSeq
See merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)dgv7861n152
Frequency
Sample Size9
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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