A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1041759



Internal ID19130978
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:72146165..72162104hg38UCSC Ensembl
Innerchr14:72612882..72628815hg19UCSC Ensembl
Innerchr14:71682635..71698568hg18UCSC Ensembl
Cytoband14q24.2
Allele length
AssemblyAllele length
hg3815940
hg1915934
hg1815934
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3531128
Samples
Known GenesRGS6
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1041759
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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