A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9951182



Internal ID3934548
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:63702773..63711221hg38UCSC Ensembl
Innerchr1:63702803..63711192hg38UCSC Ensembl
Outerchr1:63702744..63711251hg38UCSC Ensembl
chr1:64168444..64176892hg19UCSC Ensembl
Innerchr1:64168474..64176863hg19UCSC Ensembl
Outerchr1:64168415..64176922hg19UCSC Ensembl
Cytoband1p31.3
Allele length
AssemblyAllele length
hg388449
hg198449
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3586247
Supporting Variants
SamplesHG03585
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv9951182
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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