A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6331261



Internal ID9308664
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:3504090..3507481hg38UCSC Ensembl
Outerchr18:3504053..3507531hg38UCSC Ensembl
Innerchr18:3504088..3507479hg19UCSC Ensembl
Outerchr18:3504051..3507529hg19UCSC Ensembl
Cytoband18p11.31
Allele length
AssemblyAllele length
hg383479
hg193479
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2675244
Supporting Variants
SamplesNA11994
Known GenesDLGAP1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6331261
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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