A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2657423



Internal ID9923528
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:51095895..51096234hg38UCSC Ensembl
Outerchr6:51095861..51096269hg38UCSC Ensembl
Innerchr6:51063608..51063947hg19UCSC Ensembl
Outerchr6:51063574..51063982hg19UCSC Ensembl
Cytoband6p12.3
Allele length
AssemblyAllele length
hg38409
hg19409
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6135278
SamplesNA20520
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2657423
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer