A curated catalogue of human genomic structural variation




Variant Details

Variant: essv16114167



Internal ID2080750
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:1580093..1613039hg38UCSC Ensembl
Innerchr20:1580593..1612539hg38UCSC Ensembl
Outerchr20:1579093..1614039hg38UCSC Ensembl
chr20:1560739..1593685hg19UCSC Ensembl
Innerchr20:1561239..1593185hg19UCSC Ensembl
Outerchr20:1559739..1594685hg19UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg3832947
hg1932947
Variant TypeCNV loss
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3644983
Supporting Variants
SamplesHG01890
Known GenesSIRPB1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv16114167
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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