A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3760216



Internal ID18711811
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:14978756..16296799hg38UCSC Ensembl
Innerchr8:14836265..16154308hg19UCSC Ensembl
Innerchr8:14880636..16198679hg18UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg381318044
hg191318044
hg181318044
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1029399
Supporting Variants
Samples
Known GenesMSR1, SGCZ, TUSC3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3760216
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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