A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2658631



Internal ID9924736
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:39197640..39199551hg38UCSC Ensembl
Outerchr19:39197603..39199601hg38UCSC Ensembl
Innerchr19:39688280..39690191hg19UCSC Ensembl
Outerchr19:39688243..39690241hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg381999
hg191999
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5773118, essv5870619
SamplesHG01183, HG01174
Known GenesNCCRP1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2658631
Frequency
Sample Size1151
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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