A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3523869



Internal ID18822150
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:55672575..55741910hg38UCSC Ensembl
Innerchr13:56246710..56316044hg19UCSC Ensembl
Innerchr13:55144711..55214045hg18UCSC Ensembl
Cytoband13q21.1
Allele length
AssemblyAllele length
hg3869336
hg1969335
hg1869335
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1044769
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)nssv3523869
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