A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3634924



Internal ID7021724
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:73918679..73919950hg38UCSC Ensembl
Innerchr14:73918690..73919939hg38UCSC Ensembl
Outerchr14:73918668..73919961hg38UCSC Ensembl
chr14:74385382..74386653hg19UCSC Ensembl
Innerchr14:74385393..74386642hg19UCSC Ensembl
Outerchr14:74385371..74386664hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg381272
hg191272
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15060889, essv15060888
SamplesHG03771, HG03809
Known GenesZNF410
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3634924
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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