A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1013046



Internal ID18755577
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:158458793..158526817hg38UCSC Ensembl
Innerchr3:158176582..158244606hg19UCSC Ensembl
Innerchr3:159659276..159727300hg18UCSC Ensembl
Cytoband3q25.32
Allele length
AssemblyAllele length
hg3868025
hg1968025
hg1868025
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4929n100
Supporting Variantsnssv3606389, nssv3606391, nssv3606390
Samples
Known GenesRSRC1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1013046
Frequency
Sample Size29084
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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