A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2672610



Internal ID9938715
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:3635256..3636506hg38UCSC Ensembl
Outerchr18:3635219..3636556hg38UCSC Ensembl
Innerchr18:3635255..3636505hg19UCSC Ensembl
Outerchr18:3635218..3636555hg19UCSC Ensembl
Cytoband18p11.31
Allele length
AssemblyAllele length
hg381338
hg191338
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv578e199
Supporting Variantsessv5981237, essv6064531
SamplesNA19390, NA19334
Known GenesDLGAP1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2672610
Frequency
Sample Size1151
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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