A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3585520



Internal ID6973043
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:25236011..25241287hg38UCSC Ensembl
Innerchr1:25236161..25241137hg38UCSC Ensembl
Outerchr1:25235861..25241437hg38UCSC Ensembl
chr1:25562502..25567778hg19UCSC Ensembl
Innerchr1:25562652..25567628hg19UCSC Ensembl
Outerchr1:25562352..25567928hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg385277
hg195277
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9892217
SamplesHG01980
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3585520
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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