A curated catalogue of human genomic structural variation




Variant Details

Variant: essv10338698



Internal ID3740176
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:236955392..236969882hg38UCSC Ensembl
chr1:237118692..237133182hg19UCSC Ensembl
Cytoband1q43
Allele length
AssemblyAllele length
hg3814491
hg1914491
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3589226
Supporting Variants
SamplesHG03372
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv10338698
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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