A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3585570



Internal ID6973092
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:28119414..28121824hg38UCSC Ensembl
Innerchr1:28119414..28121824hg38UCSC Ensembl
Outerchr1:28119089..28122162hg38UCSC Ensembl
chr1:28445925..28448335hg19UCSC Ensembl
Innerchr1:28445925..28448335hg19UCSC Ensembl
Outerchr1:28445600..28448673hg19UCSC Ensembl
Cytoband1p35.3
Allele length
AssemblyAllele length
hg382411
hg192411
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9894559
SamplesHG00281
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3585570
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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