A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3641210



Internal ID7027984
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:72954255..72955522hg38UCSC Ensembl
Innerchr17:72954271..72955506hg38UCSC Ensembl
Outerchr17:72954239..72955538hg38UCSC Ensembl
chr17:70950394..70951661hg19UCSC Ensembl
Innerchr17:70950410..70951645hg19UCSC Ensembl
Outerchr17:70950378..70951677hg19UCSC Ensembl
Cytoband17q25.1
Allele length
AssemblyAllele length
hg381268
hg191268
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15735961
SamplesNA20535
Known GenesSLC39A11
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3641210
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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