A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3641173



Internal ID7027947
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:71411849..71417563hg38UCSC Ensembl
Innerchr17:71411849..71417563hg38UCSC Ensembl
Outerchr17:71411715..71417706hg38UCSC Ensembl
chr17:69407990..69413704hg19UCSC Ensembl
Innerchr17:69407990..69413704hg19UCSC Ensembl
Outerchr17:69407856..69413847hg19UCSC Ensembl
Cytoband17q24.3
Allele length
AssemblyAllele length
hg385715
hg195715
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15734755
SamplesHG02793
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3641173
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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