A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2669200



Internal ID9935305
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:74426106..74432247hg38UCSC Ensembl
Outerchr13:74425949..74432400hg38UCSC Ensembl
Innerchr13:75000243..75006384hg19UCSC Ensembl
Outerchr13:75000086..75006537hg19UCSC Ensembl
Cytoband13q22.1
Allele length
AssemblyAllele length
hg386452
hg196452
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6183378, essv6240833, essv6056908, essv6072336, essv5583853
SamplesNA18519, NA18856, NA18912, NA19440, NA18522
Known GenesLINC00381
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2669200
Frequency
Sample Size1151
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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