A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3489674



Internal ID18730629
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:179745112..179820975hg38UCSC Ensembl
Innerchr1:179714247..179790110hg19UCSC Ensembl
Innerchr1:177980870..178056733hg18UCSC Ensembl
Cytoband1q25.2
Allele length
AssemblyAllele length
hg3875864
hg1975864
hg1875864
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1009961
Supporting Variants
Samples
Known GenesFAM163A
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3489674
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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