A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1042513



Internal ID19131732
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:83276130..83302908hg38UCSC Ensembl
Innerchr14:83742474..83769252hg19UCSC Ensembl
Innerchr14:82812227..82839005hg18UCSC Ensembl
Cytoband14q31.2
Allele length
AssemblyAllele length
hg3826779
hg1926779
hg1826779
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3532342
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)nsv1042513
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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