A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2657105



Internal ID9576524
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:153385711..153727554hg38UCSC Ensembl
Outerchr5:153385677..153727589hg38UCSC Ensembl
Innerchr5:152765271..153107114hg19UCSC Ensembl
Outerchr5:152765237..153107149hg19UCSC Ensembl
Cytoband5q33.2
Allele length
AssemblyAllele length
hg38341913
hg19341913
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6066936, essv5812527, essv6346483
SamplesHG00699, HG00533, HG00620
Known GenesGRIA1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2657105
Frequency
Sample Size1151
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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