A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1024327



Internal ID19113544
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:20747782..20764240hg38UCSC Ensembl
Innerchr9:20747781..20764239hg19UCSC Ensembl
Innerchr9:20737781..20754239hg18UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg3816459
hg1916459
hg1816459
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3690704
Samples
Known GenesFOCAD
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1024327
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