A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1022825



Internal ID19112043
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:62729697..63578505hg38UCSC Ensembl
Innerchr5:62025524..62874332hg19UCSC Ensembl
Innerchr5:62061280..62910088hg18UCSC Ensembl
Cytoband5q12.1
Allele length
AssemblyAllele length
hg38848809
hg19848809
hg18848809
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5691n100
Supporting Variantsnssv3640782, nssv3640783, nssv3640781
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1022825
Frequency
Sample Size11257
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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