A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3641625



Internal ID6681710
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:4395845..4397619hg38UCSC Ensembl
Innerchr18:4395850..4397614hg38UCSC Ensembl
Outerchr18:4395840..4397624hg38UCSC Ensembl
chr18:4395845..4397619hg19UCSC Ensembl
Innerchr18:4395850..4397614hg19UCSC Ensembl
Outerchr18:4395840..4397624hg19UCSC Ensembl
Cytoband18p11.31
Allele length
AssemblyAllele length
hg381775
hg191775
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15781417, essv15781416
SamplesHG02861, HG03225
Known GenesDLGAP1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3641625
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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