A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15974560



Internal ID4432523
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3643459
Supporting Variants
SamplesHG03944
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15974560
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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