A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3642195



Internal ID7028965
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:35179895..35187886hg38UCSC Ensembl
Innerchr18:35179895..35187886hg38UCSC Ensembl
Outerchr18:35179761..35188034hg38UCSC Ensembl
chr18:32759859..32767850hg19UCSC Ensembl
Innerchr18:32759859..32767850hg19UCSC Ensembl
Outerchr18:32759725..32767998hg19UCSC Ensembl
Cytoband18q12.2
Allele length
AssemblyAllele length
hg387992
hg197992
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15842006, essv15842008, essv15842009, essv15842007
SamplesNA18502, NA19138, HG03352, HG02511
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3642195
Frequency
Sample Size2504
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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