A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1038792



Internal ID19128011
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:34638874..34691654hg38UCSC Ensembl
Innerchr14:35108080..35160860hg19UCSC Ensembl
Innerchr14:34177831..34230611hg18UCSC Ensembl
Cytoband14q13.1
Allele length
AssemblyAllele length
hg3852781
hg1952781
hg1852781
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1866n100
Supporting Variantsnssv3528607, nssv3528606
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)nsv1038792
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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