A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1052541



Internal ID19141760
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:79222993..79257285hg38UCSC Ensembl
Innerchr14:79689336..79723628hg19UCSC Ensembl
Innerchr14:78759089..78793381hg18UCSC Ensembl
Cytoband14q31.1
Allele length
AssemblyAllele length
hg3834293
hg1934293
hg1834293
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3531219
Samples
Known GenesNRXN3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1052541
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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