A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3645205



Internal ID7031956
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:10265096..10272840hg38UCSC Ensembl
Innerchr20:10265121..10272816hg38UCSC Ensembl
Outerchr20:10265072..10272865hg38UCSC Ensembl
chr20:10245744..10253488hg19UCSC Ensembl
Innerchr20:10245769..10253464hg19UCSC Ensembl
Outerchr20:10245720..10253513hg19UCSC Ensembl
Cytoband20p12.2
Allele length
AssemblyAllele length
hg387745
hg197745
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16141897
SamplesNA19025
Known GenesSNAP25
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3645205
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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