A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3585267



Internal ID6625587
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:13896407..13901691hg38UCSC Ensembl
Innerchr1:13896455..13901643hg38UCSC Ensembl
Outerchr1:13896359..13901739hg38UCSC Ensembl
chr1:14222902..14228186hg19UCSC Ensembl
Innerchr1:14222950..14228138hg19UCSC Ensembl
Outerchr1:14222854..14228234hg19UCSC Ensembl
Cytoband1p36.21
Allele length
AssemblyAllele length
hg385285
hg195285
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9860509
SamplesHG03784
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3585267
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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