A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3645713



Internal ID7032462
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:35259639..35262527hg38UCSC Ensembl
Innerchr20:35259639..35262527hg38UCSC Ensembl
Outerchr20:35259478..35262702hg38UCSC Ensembl
chr20:33847442..33850330hg19UCSC Ensembl
Innerchr20:33847442..33850330hg19UCSC Ensembl
Outerchr20:33847281..33850505hg19UCSC Ensembl
Cytoband20q11.22
Allele length
AssemblyAllele length
hg382889
hg192889
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16178647
SamplesNA21120
Known GenesMMP24
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3645713
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