A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3502273



Internal ID18800554
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:163773199..163918955hg38UCSC Ensembl
Innerchr1:163742436..163888192hg19UCSC Ensembl
Innerchr1:162009060..162154816hg18UCSC Ensembl
Cytoband1q23.3
Allele length
AssemblyAllele length
hg38145757
hg19145757
hg18145757
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1000322
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3502273
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