A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3506248



Internal ID18804529
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:97103220..97175867hg38UCSC Ensembl
Innerchr11:96974220..97046867hg19UCSC Ensembl
Innerchr11:96479430..96552077hg18UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg3872648
hg1972648
hg1872648
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1043735
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)nssv3506248
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