A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2675710



Internal ID9595129
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 StatusM
Merged Variants
Supporting Variantsessv6089253, essv6327680, essv5747965, essv6320790, essv6062824, essv6050737, essv6515449, essv5997827, essv6530651, essv5957441, essv5398974, essv6272133, essv6003523, essv6055024, essv6200017
SamplesHG01359, HG01075, HG01055, HG01365, HG01375, NA18856, NA19440, HG01069, HG01080, HG00534, NA19452, HG00566, HG01374, HG00702, HG00361
Known GenesROBO2
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2675710
Frequency
Sample Size1151
Observed Gain0
Observed Loss15
Observed Complex0
Frequencyn/a


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