A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2669024



Internal ID9935129
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:157876368..157877570hg38UCSC Ensembl
chr5:157303376..157304578hg19UCSC Ensembl
Cytoband5q33.3
Allele length
AssemblyAllele length
hg381203
hg191203
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6332132
SamplesHG00464
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2669024
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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