A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3657426



Internal ID18609021
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:36550916..39052434hg38UCSC Ensembl
Innerchr6:36518693..39020210hg19UCSC Ensembl
Innerchr6:36626671..39128188hg18UCSC Ensembl
Cytoband6p21.2
Allele length
AssemblyAllele length
hg382501519
hg192501518
hg182501518
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1015689
Supporting Variants
Samples
Known GenesBTBD9, C6orf89, CCDC167, CDKN1A, CMTR1, CPNE5, DNAH8, FGD2, GLO1, GLP1R, LOC100131047, MDGA1, MIR3925, MIR4462, MTCH1, PI16, PIM1, PPIL1, RAB44, RNF8, SRSF3, TBC1D22B, TMEM217, ZFAND3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3657426
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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