A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3585487



Internal ID6625805
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:23670929..23671231hg38UCSC Ensembl
Innerchr1:23670939..23671222hg38UCSC Ensembl
Outerchr1:23670920..23671241hg38UCSC Ensembl
chr1:23997419..23997721hg19UCSC Ensembl
Innerchr1:23997429..23997712hg19UCSC Ensembl
Outerchr1:23997410..23997731hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg38303
hg19303
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9890046
SamplesNA19679
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3585487
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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