A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1043886



Internal ID18786417
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 StatusM
Merged Variants
Supporting Variantsnssv3713288
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)nsv1043886
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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