A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3681652



Internal ID18979933
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:8197726..8292820hg38UCSC Ensembl
Innerchr8:8055248..8150342hg19UCSC Ensembl
Innerchr8:8092658..8187752hg18UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg3895095
hg1995095
hg1895095
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1021458
Supporting Variants
Samples
Known GenesFAM86B3P
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3681652
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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