A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3584826



Internal ID18536421
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:42652464..44431352hg38UCSC Ensembl
Innerchr20:41281104..43059992hg19UCSC Ensembl
Innerchr20:40714518..42493406hg18UCSC Ensembl
Cytoband20q12
Allele length
AssemblyAllele length
hg381778889
hg191778889
hg181778889
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1057847
Supporting Variants
Samples
Known GenesFITM2, GDAP1L1, GTSF1L, HNF4A, IFT52, JPH2, L3MBTL1, MIR3646, MYBL2, OSER1, OSER1-AS1, PTPRT, R3HDML, SGK2, SRSF6, TOX2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3584826
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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