A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3488808



Internal ID18729763
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:172284625..172335550hg38UCSC Ensembl
Innerchr1:172253765..172304690hg19UCSC Ensembl
Innerchr1:170520388..170571313hg18UCSC Ensembl
Cytoband1q24.3
Allele length
AssemblyAllele length
hg3850926
hg1950926
hg1850926
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1006542
Supporting Variants
Samples
Known GenesDNM3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3488808
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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