A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3607969



Internal ID18906250
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:162567179..162730030hg38UCSC Ensembl
Innerchr3:162284967..162447818hg19UCSC Ensembl
Innerchr3:163767661..163930512hg18UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg38162852
hg19162852
hg18162852
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1005142
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)nssv3607969
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