A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2671636



Internal ID4715970
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:48936135..48938507hg19UCSC Ensembl
Outerchr19:48936098..48938557hg19UCSC Ensembl
Cytoband19q13.33
Allele length
AssemblyAllele length
hg19n/a
Variant TypeCNV Deletion
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsessv6084398
SamplesNA19429
Known GenesGRIN2D
Method
Analysis
Platform
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2671636
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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