A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1040418



Internal ID19129637
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:39824296..39870324hg38UCSC Ensembl
Innerchr14:40293500..40339528hg19UCSC Ensembl
Innerchr14:39363251..39409279hg18UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg3846029
hg1946029
hg1846029
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3712290
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)nsv1040418
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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