A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1044881



Internal ID19134100
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:66521753..66552564hg38UCSC Ensembl
Innerchr13:67095885..67126696hg19UCSC Ensembl
Innerchr13:65993886..66024697hg18UCSC Ensembl
Cytoband13q21.32
Allele length
AssemblyAllele length
hg3830812
hg1930812
hg1830812
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3527922
Samples
Known GenesPCDH9
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1044881
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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