A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1024948



Internal ID18767480
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:19189215..19248346hg38UCSC Ensembl
Innerchr9:19189213..19248344hg19UCSC Ensembl
Innerchr9:19179213..19238344hg18UCSC Ensembl
Cytoband9p22.1
Allele length
AssemblyAllele length
hg3859132
hg1959132
hg1859132
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3755828
Samples
Known GenesDENND4C
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1024948
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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