A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3635402



Internal ID7022201
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 State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15103409
SamplesNA18549
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3635402
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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