A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2677751



Internal ID9943856
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:153729226..153948485hg38UCSC Ensembl
Outerchr5:153729192..153948520hg38UCSC Ensembl
Innerchr5:153108786..153328045hg19UCSC Ensembl
Outerchr5:153108752..153328080hg19UCSC Ensembl
Cytoband5q33.2
Allele length
AssemblyAllele length
hg38219329
hg19219329
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6144264
SamplesHG00500
Known GenesGRIA1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2677751
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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