A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3635352



Internal ID7022151
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:93118350..93129254hg38UCSC Ensembl
Innerchr14:93118850..93128754hg38UCSC Ensembl
Outerchr14:93117350..93130254hg38UCSC Ensembl
chr14:93584695..93595599hg19UCSC Ensembl
Innerchr14:93585195..93595099hg19UCSC Ensembl
Outerchr14:93583695..93596599hg19UCSC Ensembl
Cytoband14q32.12
Allele length
AssemblyAllele length
hg3810905
hg1910905
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15098876
SamplesNA19207
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3635352
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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