A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3713288



Internal ID18664883
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:99038252..99112843hg38UCSC Ensembl
Innerchr13:99690506..99765097hg19UCSC Ensembl
Innerchr13:98488507..98563098hg18UCSC Ensembl
Cytoband13q32.3
Allele length
AssemblyAllele length
hg3874592
hg1974592
hg1874592
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1043886
Supporting Variants
Samples
Known GenesDOCK9, DOCK9-AS2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3713288
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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