A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3643459



Internal ID7030221
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:3219424..3224625hg38UCSC Ensembl
Innerchr19:3219924..3224125hg38UCSC Ensembl
Outerchr19:3218424..3225625hg38UCSC Ensembl
chr19:3219422..3224623hg19UCSC Ensembl
Innerchr19:3219922..3224123hg19UCSC Ensembl
Outerchr19:3218422..3225623hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg385202
hg195202
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15974557, essv15974559, essv15974560, essv15974558
SamplesHG03944, HG03885, HG03940, HG03695
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3643459
Frequency
Sample Size2504
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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