A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3726075



Internal ID19024356
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:51189048..51227206hg38UCSC Ensembl
Innerchr18:48715418..48753576hg19UCSC Ensembl
Innerchr18:46969416..47007574hg18UCSC Ensembl
Cytoband18q21.2
Allele length
AssemblyAllele length
hg3838159
hg1938159
hg1838159
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1055468
Supporting Variants
Samples
Known GenesMEX3C
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3726075
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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