A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3599357



Internal ID18550952
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:5432523..5731197hg38UCSC Ensembl
Innerchr20:5413169..5711843hg19UCSC Ensembl
Innerchr20:5361169..5659843hg18UCSC Ensembl
Cytoband20p12.3
Allele length
AssemblyAllele length
hg38298675
hg19298675
hg18298675
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1065497
Supporting Variants
Samples
Known GenesGPCPD1, LINC00654, LINC00658, LOC643406
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3599357
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer