A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6423435



Internal ID9440668
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:153304529..153312748hg38UCSC Ensembl
Outerchr5:153304492..153312798hg38UCSC Ensembl
Innerchr5:152684089..152692308hg19UCSC Ensembl
Outerchr5:152684052..152692358hg19UCSC Ensembl
Cytoband5q33.1
Allele length
AssemblyAllele length
hg388307
hg198307
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2663837
Supporting Variants
SamplesNA18638
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6423435
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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