A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3634077



Internal ID7020881
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:36755612..36757421hg38UCSC Ensembl
Innerchr14:36755650..36757384hg38UCSC Ensembl
Outerchr14:36755575..36757459hg38UCSC Ensembl
chr14:37224817..37226626hg19UCSC Ensembl
Innerchr14:37224855..37226589hg19UCSC Ensembl
Outerchr14:37224780..37226664hg19UCSC Ensembl
Cytoband14q13.3
Allele length
AssemblyAllele length
hg381810
hg191810
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14969770
SamplesHG04206
Known GenesSLC25A21
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3634077
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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