A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3635580



Internal ID7022379
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:103200275..103247803hg38UCSC Ensembl
Innerchr14:103200775..103247303hg38UCSC Ensembl
Outerchr14:103199275..103248803hg38UCSC Ensembl
chr14:103666612..103714140hg19UCSC Ensembl
Innerchr14:103667112..103713640hg19UCSC Ensembl
Outerchr14:103665612..103715140hg19UCSC Ensembl
Cytoband14q32.32
Allele length
AssemblyAllele length
hg3847529
hg1947529
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv421e214
Supporting Variantsessv15114224
SamplesHG01806
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3635580
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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