A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3595672



Internal ID6982990
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:27654329..27656634hg38UCSC Ensembl
Innerchr3:27654479..27656484hg38UCSC Ensembl
Outerchr3:27654179..27656784hg38UCSC Ensembl
chr3:27695820..27698125hg19UCSC Ensembl
Innerchr3:27695970..27697975hg19UCSC Ensembl
Outerchr3:27695670..27698275hg19UCSC Ensembl
Cytoband3p24.1
Allele length
AssemblyAllele length
hg382306
hg192306
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv10961161
SamplesNA18964
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3595672
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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