A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1044688



Internal ID19133907
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:18592436..18844391hg38UCSC Ensembl
Innerchr13:19166576..19418531hg19UCSC Ensembl
Innerchr13:18064576..18316531hg18UCSC Ensembl
Cytoband13q11
Allele length
AssemblyAllele length
hg38251956
hg19251956
hg18251956
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1603n100
Supporting Variantsnssv3714928
Samples
Known GenesANKRD20A9P, LINC00417
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1044688
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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