A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3585759



Internal ID6973280
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:37709878..37717161hg38UCSC Ensembl
Innerchr1:37709878..37717161hg38UCSC Ensembl
Outerchr1:37709828..37717216hg38UCSC Ensembl
chr1:38175550..38182833hg19UCSC Ensembl
Innerchr1:38175550..38182833hg19UCSC Ensembl
Outerchr1:38175500..38182888hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg387284
hg197284
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9912708, essv9912709
SamplesNA19314, NA19404
Known GenesEPHA10
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3585759
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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