A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3585707



Internal ID6973227
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:34450498..34456788hg38UCSC Ensembl
Innerchr1:34450532..34456755hg38UCSC Ensembl
Outerchr1:34450465..34456822hg38UCSC Ensembl
chr1:34916099..34922389hg19UCSC Ensembl
Innerchr1:34916133..34922356hg19UCSC Ensembl
Outerchr1:34916066..34922423hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg386291
hg196291
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9899042
SamplesHG02922
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3585707
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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