A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3640662



Internal ID7027436
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:45360617..45364337hg38UCSC Ensembl
Innerchr17:45360630..45364324hg38UCSC Ensembl
Outerchr17:45360604..45364350hg38UCSC Ensembl
chr17:43437983..43441703hg19UCSC Ensembl
Innerchr17:43437996..43441690hg19UCSC Ensembl
Outerchr17:43437970..43441716hg19UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg383721
hg193721
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15680909
SamplesHG02660
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3640662
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer