A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3635395



Internal ID7022194
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:94989635..94991744hg38UCSC Ensembl
Innerchr14:94989642..94991738hg38UCSC Ensembl
Outerchr14:94989629..94991751hg38UCSC Ensembl
chr14:95455972..95458081hg19UCSC Ensembl
Innerchr14:95455979..95458075hg19UCSC Ensembl
Outerchr14:95455966..95458088hg19UCSC Ensembl
Cytoband14q32.13
Allele length
AssemblyAllele length
hg382110
hg192110
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15103362, essv15103363
SamplesHG01990, HG02010
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3635395
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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