A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3634789



Internal ID6674904
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:66592062..66643006hg38UCSC Ensembl
Innerchr14:66592086..66642982hg38UCSC Ensembl
Outerchr14:66592038..66643030hg38UCSC Ensembl
chr14:67058780..67109724hg19UCSC Ensembl
Innerchr14:67058804..67109700hg19UCSC Ensembl
Outerchr14:67058756..67109748hg19UCSC Ensembl
Cytoband14q23.3
Allele length
AssemblyAllele length
hg3850945
hg1950945
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15046047, essv15046048
SamplesHG02895, HG03717
Known GenesGPHN
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3634789
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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