A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3726077



Internal ID19024358
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:51366466..51428797hg38UCSC Ensembl
Innerchr18:48892836..48955167hg19UCSC Ensembl
Innerchr18:47146834..47209165hg18UCSC Ensembl
Cytoband18q21.2
Allele length
AssemblyAllele length
hg3862332
hg1962332
hg1862332
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1057935
Supporting Variants
Samples
Known GenesLOC100287225
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3726077
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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