A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3645808



Internal ID7032556
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:39424381..39431215hg38UCSC Ensembl
Innerchr20:39424411..39431185hg38UCSC Ensembl
Outerchr20:39424351..39431245hg38UCSC Ensembl
chr20:38053024..38059858hg19UCSC Ensembl
Innerchr20:38053054..38059828hg19UCSC Ensembl
Outerchr20:38052994..38059888hg19UCSC Ensembl
Cytoband20q12
Allele length
AssemblyAllele length
hg386835
hg196835
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16185317, essv16185316
SamplesHG02131, HG00613
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3645808
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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