A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1014624



Internal ID18757159
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:46421933..46507698hg38UCSC Ensembl
Innerchr3:46463424..46549188hg19UCSC Ensembl
Innerchr3:46438428..46524192hg18UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg3885766
hg1985765
hg1885765
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3589738
Samples
Known GenesLTF, RTP3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1014624
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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