A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1043109



Internal ID18785640
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:57545677..57618153hg38UCSC Ensembl
Innerchr14:58012395..58084871hg19UCSC Ensembl
Innerchr14:57082148..57154624hg18UCSC Ensembl
Cytoband14q22.3
Allele length
AssemblyAllele length
hg3872477
hg1972477
hg1872477
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3713496
Samples
Known GenesSLC35F4
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1043109
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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