A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3633238



Internal ID6673360
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:95124249..95137834hg38UCSC Ensembl
Innerchr13:95124749..95137334hg38UCSC Ensembl
Outerchr13:95123249..95138834hg38UCSC Ensembl
chr13:95776503..95790088hg19UCSC Ensembl
Innerchr13:95777003..95789588hg19UCSC Ensembl
Outerchr13:95775503..95791088hg19UCSC Ensembl
Cytoband13q32.1
Allele length
AssemblyAllele length
hg3813586
hg1913586
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14868828
SamplesHG04076
Known GenesABCC4
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3633238
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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