A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1046932



Internal ID19136151
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:39662932..39798881hg38UCSC Ensembl
Innerchr14:40132136..40268085hg19UCSC Ensembl
Innerchr14:39201887..39337836hg18UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg38135950
hg19135950
hg18135950
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3530129
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)nsv1046932
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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