A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1038432



Internal ID19127651
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:47801072..47893881hg38UCSC Ensembl
Innerchr14:48270275..48363084hg19UCSC Ensembl
Innerchr14:47340025..47432834hg18UCSC Ensembl
Cytoband14q21.3
Allele length
AssemblyAllele length
hg3892810
hg1992810
hg1892810
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3713485
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)nsv1038432
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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