A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1044363



Internal ID19133582
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:65384114..65403410hg38UCSC Ensembl
Innerchr14:65850832..65870128hg19UCSC Ensembl
Innerchr14:64920585..64939881hg18UCSC Ensembl
Cytoband14q23.3
Allele length
AssemblyAllele length
hg3819297
hg1919297
hg1819297
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3531081
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1044363
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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