A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1034905



Internal ID18777437
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:38938562..39017379hg38UCSC Ensembl
Innerchr5:38938664..39017481hg19UCSC Ensembl
Innerchr5:38974421..39053238hg18UCSC Ensembl
Cytoband5p13.1
Allele length
AssemblyAllele length
hg3878818
hg1978818
hg1878818
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5636n100
Supporting Variantsnssv3637099
Samples
Known GenesRICTOR
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1034905
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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