A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3723223



Internal ID19021504
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:73215948..73402935hg38UCSC Ensembl
Innerchr18:70883183..71070170hg19UCSC Ensembl
Innerchr18:69034163..69221150hg18UCSC Ensembl
Cytoband18q22.3
Allele length
AssemblyAllele length
hg38186988
hg19186988
hg18186988
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1060830
Supporting Variants
Samples
Known GenesLOC100505817, LOC400655
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3723223
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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