A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6134103



Internal ID9111506
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 Flag1
Merged StatusS
Merged Variantsesv2671513
Supporting Variants
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)essv6134103
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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