A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2678521



Internal ID9597940
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:9325164..9325490hg38UCSC Ensembl
Outerchr19:9325127..9325540hg38UCSC Ensembl
Innerchr19:9435840..9436166hg19UCSC Ensembl
Outerchr19:9435803..9436216hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg38414
hg19414
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6097559, essv6356042, essv5757631
SamplesHG00258, NA19700, NA19657
Known GenesZNF559, ZNF559-ZNF177
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2678521
Frequency
Sample Size1151
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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