A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3635644



Internal ID6675755
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:105428222..105429463hg38UCSC Ensembl
Innerchr14:105428272..105429413hg38UCSC Ensembl
Outerchr14:105428172..105429513hg38UCSC Ensembl
chr14:105894559..105895800hg19UCSC Ensembl
Innerchr14:105894609..105895750hg19UCSC Ensembl
Outerchr14:105894509..105895850hg19UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg381242
hg191242
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15117410, essv15117409
SamplesNA19317, NA19043
Known GenesMTA1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3635644
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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