A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3634656



Internal ID7021459
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:59844007..59845090hg38UCSC Ensembl
Innerchr14:59844007..59845090hg38UCSC Ensembl
Outerchr14:59843796..59845320hg38UCSC Ensembl
chr14:60310725..60311808hg19UCSC Ensembl
Innerchr14:60310725..60311808hg19UCSC Ensembl
Outerchr14:60310514..60312038hg19UCSC Ensembl
Cytoband14q23.1
Allele length
AssemblyAllele length
hg381084
hg191084
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15027657
SamplesNA18990
Known GenesRTN1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3634656
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer