A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3641610



Internal ID6681695
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:3856566..3859970hg38UCSC Ensembl
Innerchr18:3857066..3859470hg38UCSC Ensembl
Outerchr18:3855566..3860970hg38UCSC Ensembl
chr18:3856566..3859970hg19UCSC Ensembl
Innerchr18:3857066..3859470hg19UCSC Ensembl
Outerchr18:3855566..3860970hg19UCSC Ensembl
Cytoband18p11.31
Allele length
AssemblyAllele length
hg383405
hg193405
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15780302
SamplesHG02973
Known GenesDLGAP1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3641610
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