A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3643025



Internal ID7029794
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:71617097..71679919hg38UCSC Ensembl
Innerchr18:71617127..71679889hg38UCSC Ensembl
Outerchr18:71617067..71679949hg38UCSC Ensembl
chr18:69284333..69347155hg19UCSC Ensembl
Innerchr18:69284363..69347125hg19UCSC Ensembl
Outerchr18:69284303..69347185hg19UCSC Ensembl
Cytoband18q22.3
Allele length
AssemblyAllele length
hg3862823
hg1962823
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv636e214
Supporting Variantsessv15932166, essv15932163, essv15932164, essv15932165
SamplesNA06984, HG03061, HG03397, HG00329
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3643025
Frequency
Sample Size2504
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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