A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1048794



Internal ID19138013
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:68147435..68182514hg38UCSC Ensembl
Innerchr14:68614152..68649231hg19UCSC Ensembl
Innerchr14:67683905..67718984hg18UCSC Ensembl
Cytoband14q24.1
Allele length
AssemblyAllele length
hg3835080
hg1935080
hg1835080
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3531106
Samples
Known GenesRAD51B
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1048794
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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