A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1053520



Internal ID19142739
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:72018478..72070485hg38UCSC Ensembl
Innerchr14:72485195..72537202hg19UCSC Ensembl
Innerchr14:71554948..71606955hg18UCSC Ensembl
Cytoband14q24.2
Allele length
AssemblyAllele length
hg3852008
hg1952008
hg1852008
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3713525
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)nsv1053520
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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