A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3641249



Internal ID6681334
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:74883373..74884443hg38UCSC Ensembl
Innerchr17:74883373..74884443hg38UCSC Ensembl
Outerchr17:74883297..74884519hg38UCSC Ensembl
chr17:72879503..72880573hg19UCSC Ensembl
Innerchr17:72879503..72880573hg19UCSC Ensembl
Outerchr17:72879427..72880649hg19UCSC Ensembl
Cytoband17q25.1
Allele length
AssemblyAllele length
hg381071
hg191071
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15740483
SamplesNA18501
Known GenesFADS6
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3641249
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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