A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1038384



Internal ID19127603
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:44977984..45052380hg38UCSC Ensembl
Innerchr14:45447187..45521583hg19UCSC Ensembl
Innerchr14:44516937..44591333hg18UCSC Ensembl
Cytoband14q21.2
Allele length
AssemblyAllele length
hg3874397
hg1974397
hg1874397
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3530441
Samples
Known GenesFAM179B
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1038384
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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