A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3588095



Internal ID6975519
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:182103286..182110357hg38UCSC Ensembl
Innerchr1:182103286..182110357hg38UCSC Ensembl
Outerchr1:182102786..182110857hg38UCSC Ensembl
chr1:182072421..182079492hg19UCSC Ensembl
Innerchr1:182072421..182079492hg19UCSC Ensembl
Outerchr1:182071921..182079992hg19UCSC Ensembl
Cytoband1q25.3
Allele length
AssemblyAllele length
hg387072
hg197072
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv10207564
SamplesNA19380
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3588095
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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