A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1009961



Internal ID18752492
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 StatusM
Merged Variantsdgv472n100
Supporting Variantsnssv3489674
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)nsv1009961
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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