A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3634510



Internal ID7021313
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:51924967..51929601hg38UCSC Ensembl
Innerchr14:51924967..51929601hg38UCSC Ensembl
Outerchr14:51924850..51929717hg38UCSC Ensembl
chr14:52391685..52396319hg19UCSC Ensembl
Innerchr14:52391685..52396319hg19UCSC Ensembl
Outerchr14:52391568..52396435hg19UCSC Ensembl
Cytoband14q22.1
Allele length
AssemblyAllele length
hg384635
hg194635
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15010571
SamplesNA19901
Known GenesGNG2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3634510
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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