A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3641330



Internal ID7028104
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:78291364..78293922hg38UCSC Ensembl
Innerchr17:78291394..78293893hg38UCSC Ensembl
Outerchr17:78291335..78293952hg38UCSC Ensembl
chr17:76287445..76290003hg19UCSC Ensembl
Innerchr17:76287475..76289974hg19UCSC Ensembl
Outerchr17:76287416..76290033hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg382559
hg192559
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15751286
SamplesNA20908
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3641330
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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