A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3587508



Internal ID6627810
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:150612667..150621525hg38UCSC Ensembl
Innerchr1:150612817..150621375hg38UCSC Ensembl
Outerchr1:150612517..150621675hg38UCSC Ensembl
chr1:150585143..150594001hg19UCSC Ensembl
Innerchr1:150585293..150593851hg19UCSC Ensembl
Outerchr1:150584993..150594151hg19UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg388859
hg198859
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv10145179
SamplesHG03684
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3587508
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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