A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1021803



Internal ID19111021
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:58014541..58037694hg38UCSC Ensembl
Innerchr5:57310368..57333521hg19UCSC Ensembl
Innerchr5:57346125..57369278hg18UCSC Ensembl
Cytoband5q11.2
Allele length
AssemblyAllele length
hg3823154
hg1923154
hg1823154
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3745983, nssv3642169, nssv3642166, nssv3642168, nssv3642164, nssv3642167, nssv3642165, nssv3642170
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)nsv1021803
Frequency
Sample Size11257
Observed Gain1
Observed Loss7
Observed Complex0
Frequencyn/a


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