A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3634753



Internal ID6674868
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:64507850..64510486hg38UCSC Ensembl
Innerchr14:64507850..64510486hg38UCSC Ensembl
Outerchr14:64507637..64510671hg38UCSC Ensembl
chr14:64974568..64977204hg19UCSC Ensembl
Innerchr14:64974568..64977204hg19UCSC Ensembl
Outerchr14:64974355..64977389hg19UCSC Ensembl
Cytoband14q23.3
Allele length
AssemblyAllele length
hg382637
hg192637
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15040772
SamplesHG01864
Known GenesZBTB1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3634753
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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