A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3635471



Internal ID7022270
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:98711855..98730148hg38UCSC Ensembl
chr14:99178192..99196485hg19UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg3818294
hg1918294
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv419e214
Supporting Variantsessv15106770, essv15106771, essv15106766, essv15106769, essv15106767, essv15106765, essv15106768
SamplesHG01066, NA20752, HG01325, HG01064, NA20811, HG01697, HG01631
Known GenesC14orf177
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3635471
Frequency
Sample Size2504
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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