A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3616725



Internal ID6656921
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:27659793..27661170hg38UCSC Ensembl
Innerchr8:27659808..27661156hg38UCSC Ensembl
Outerchr8:27659779..27661185hg38UCSC Ensembl
chr8:27517310..27518687hg19UCSC Ensembl
Innerchr8:27517325..27518673hg19UCSC Ensembl
Outerchr8:27517296..27518702hg19UCSC Ensembl
Cytoband8p21.1
Allele length
AssemblyAllele length
hg381378
hg191378
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13150587, essv13150588
SamplesHG02952, HG03559
Known GenesSCARA3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3616725
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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