A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15734068



Internal ID5920699
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:71071622..71072679hg38UCSC Ensembl
Innerchr17:71071671..71072631hg38UCSC Ensembl
Outerchr17:71071574..71072728hg38UCSC Ensembl
chr17:69067763..69068820hg19UCSC Ensembl
Innerchr17:69067812..69068772hg19UCSC Ensembl
Outerchr17:69067715..69068869hg19UCSC Ensembl
Cytoband17q24.3
Allele length
AssemblyAllele length
hg381058
hg191058
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3641168
Supporting Variants
SamplesNA19331
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15734068
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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