A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1020813



Internal ID18763347
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:155474295..155498618hg38UCSC Ensembl
Innerchr5:154853855..154878178hg19UCSC Ensembl
Innerchr5:154834048..154858371hg18UCSC Ensembl
Cytoband5q33.2
Allele length
AssemblyAllele length
hg3824324
hg1924324
hg1824324
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5821n100
Supporting Variantsnssv3648200
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)nsv1020813
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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