A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1036738



Internal ID18779269
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:95140842..95292222hg38UCSC Ensembl
Innerchr14:95607179..95758559hg19UCSC Ensembl
Innerchr14:94676932..94828312hg18UCSC Ensembl
Cytoband14q32.13
Allele length
AssemblyAllele length
hg38151381
hg19151381
hg18151381
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3532622
Samples
Known GenesCLMN, DICER1, DICER1-AS1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1036738
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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