A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3585490



Internal ID6973013
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:23714346..23721625hg38UCSC Ensembl
Innerchr1:23714496..23721475hg38UCSC Ensembl
Outerchr1:23714196..23721775hg38UCSC Ensembl
chr1:24040836..24048115hg19UCSC Ensembl
Innerchr1:24040986..24047965hg19UCSC Ensembl
Outerchr1:24040686..24048265hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg387280
hg197280
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9890058
SamplesHG04212
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3585490
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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