A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3641037



Internal ID7027811
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:65125356..65126547hg38UCSC Ensembl
Innerchr17:65125392..65126511hg38UCSC Ensembl
Outerchr17:65125320..65126583hg38UCSC Ensembl
chr17:63121474..63122665hg19UCSC Ensembl
Innerchr17:63121510..63122629hg19UCSC Ensembl
Outerchr17:63121438..63122701hg19UCSC Ensembl
Cytoband17q24.1
Allele length
AssemblyAllele length
hg381192
hg191192
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15724801
SamplesHG03479
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3641037
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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