A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3640650



Internal ID7027425
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:44578936..44594726hg38UCSC Ensembl
Innerchr17:44578936..44594726hg38UCSC Ensembl
Outerchr17:44578436..44595226hg38UCSC Ensembl
chr17:42656304..42672094hg19UCSC Ensembl
Innerchr17:42656304..42672094hg19UCSC Ensembl
Outerchr17:42655804..42672594hg19UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg3815791
hg1915791
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15680772
SamplesHG02604
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3640650
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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