A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3687461



Internal ID18985742
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:47254831..47334731hg38UCSC Ensembl
Innerchr8:48167423..48247297hg19UCSC Ensembl
Innerchr8:48329976..48409850hg18UCSC Ensembl
Cytoband8q11.21
Allele length
AssemblyAllele length
hg3879901
hg1979875
hg1879875
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1030486
Supporting Variants
Samples
Known GenesSPIDR
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3687461
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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