A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6426925



Internal ID9235555
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:74927263..74928105hg38UCSC Ensembl
Outerchr5:74927226..74928155hg38UCSC Ensembl
Innerchr5:74223088..74223930hg19UCSC Ensembl
Outerchr5:74223051..74223980hg19UCSC Ensembl
Cytoband5q13.3
Allele length
AssemblyAllele length
hg38930
hg19930
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2662892
Supporting Variants
SamplesNA11932
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6426925
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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