A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3646311



Internal ID7033056
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:63373220..63391727hg38UCSC Ensembl
Innerchr20:63373720..63391227hg38UCSC Ensembl
Outerchr20:63372220..63392727hg38UCSC Ensembl
chr20:62004572..62023080hg19UCSC Ensembl
Innerchr20:62005072..62022580hg19UCSC Ensembl
Outerchr20:62003572..62024080hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg3818508
hg1918509
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv791e214
Supporting Variantsessv16229468
SamplesHG01462
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3646311
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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