A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6272133



Internal ID9249536
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:77293592..77294433hg38UCSC Ensembl
Outerchr3:77293555..77294483hg38UCSC Ensembl
Innerchr3:77342743..77343584hg19UCSC Ensembl
Outerchr3:77342706..77343634hg19UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg38929
hg19929
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2675710
Supporting Variants
SamplesHG01075
Known GenesROBO2
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6272133
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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