A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3725299



Internal ID19023580
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:23324442..23369806hg38UCSC Ensembl
Innerchr18:20904406..20949770hg19UCSC Ensembl
Innerchr18:19158404..19203768hg18UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg3845365
hg1945365
hg1845365
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1060220
Supporting Variants
Samples
Known GenesTMEM241
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3725299
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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