A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3725300



Internal ID18676895
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:23769083..23913926hg38UCSC Ensembl
Innerchr18:21349047..21493890hg19UCSC Ensembl
Innerchr18:19603045..19747888hg18UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg38144844
hg19144844
hg18144844
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1060031
Supporting Variants
Samples
Known GenesLAMA3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3725300
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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