A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2671513



Internal ID9590932
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:22008496..23001069hg38UCSC Ensembl
chr19:22191298..23183871hg19UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg38992574
hg19992574
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv633e199
Supporting Variantsessv6134103
SamplesNA19434
Known GenesLOC100996349, LOC440518, ZNF208, ZNF257, ZNF492, ZNF676, ZNF728, ZNF729, ZNF98, ZNF99
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2671513
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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