A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3643457



Internal ID7030219
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:3130375..3131782hg38UCSC Ensembl
Innerchr19:3130401..3131756hg38UCSC Ensembl
Outerchr19:3130349..3131808hg38UCSC Ensembl
chr19:3130373..3131780hg19UCSC Ensembl
Innerchr19:3130399..3131754hg19UCSC Ensembl
Outerchr19:3130347..3131806hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg381408
hg191408
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15974552, essv15974553
SamplesNA18954, HG00672
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3643457
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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