A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1043542



Internal ID19132761
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:42430859..42523219hg38UCSC Ensembl
Innerchr14:42900062..42992422hg19UCSC Ensembl
Innerchr14:41969812..42062172hg18UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg3892361
hg1992361
hg1892361
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1887n100
Supporting Variantsnssv3530208, nssv3530209
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)nsv1043542
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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