A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3641075



Internal ID7027849
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:66943931..66944979hg38UCSC Ensembl
Innerchr17:66943931..66944979hg38UCSC Ensembl
Outerchr17:66943628..66945245hg38UCSC Ensembl
chr17:64940048..64941095hg19UCSC Ensembl
Innerchr17:64940048..64941095hg19UCSC Ensembl
Outerchr17:64939745..64941361hg19UCSC Ensembl
Cytoband17q24.2
Allele length
AssemblyAllele length
hg381049
hg191048
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15726458, essv15726459, essv15726461, essv15726462, essv15726460
SamplesNA19076, HG01849, HG00419, NA18553, NA19072
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3641075
Frequency
Sample Size2504
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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