A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15103409



Internal ID5093722
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:95545669..95547832hg38UCSC Ensembl
Innerchr14:95545669..95547832hg38UCSC Ensembl
Outerchr14:95545433..95548125hg38UCSC Ensembl
chr14:96012006..96014169hg19UCSC Ensembl
Innerchr14:96012006..96014169hg19UCSC Ensembl
Outerchr14:96011770..96014462hg19UCSC Ensembl
Cytoband14q32.13
Allele length
AssemblyAllele length
hg382164
hg192164
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3635402
Supporting Variants
SamplesNA18549
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15103409
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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