A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2665596



Internal ID9931701
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:46763105..46766076hg38UCSC Ensembl
Outerchr19:46763068..46766126hg38UCSC Ensembl
Innerchr19:47266362..47269333hg19UCSC Ensembl
Outerchr19:47266325..47269383hg19UCSC Ensembl
Cytoband19q13.32
Allele length
AssemblyAllele length
hg383059
hg193059
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6458733
SamplesHG00608
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2665596
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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