A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3634944



Internal ID7021744
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:74458650..74460317hg38UCSC Ensembl
Innerchr14:74458693..74460274hg38UCSC Ensembl
Outerchr14:74458607..74460360hg38UCSC Ensembl
chr14:74925353..74927020hg19UCSC Ensembl
Innerchr14:74925396..74926977hg19UCSC Ensembl
Outerchr14:74925310..74927063hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg381668
hg191668
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15061247
SamplesNA18517
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3634944
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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