A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3644153



Internal ID7030909
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:31794555..31802392hg38UCSC Ensembl
Innerchr19:31794566..31802381hg38UCSC Ensembl
Outerchr19:31794544..31802403hg38UCSC Ensembl
chr19:32285461..32293298hg19UCSC Ensembl
Innerchr19:32285472..32293287hg19UCSC Ensembl
Outerchr19:32285450..32293309hg19UCSC Ensembl
Cytoband19q12
Allele length
AssemblyAllele length
hg387838
hg197838
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16039953
SamplesHG03971
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3644153
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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