A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1029733



Internal ID19118952
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:15520..68548hg38UCSC Ensembl
Innerchr5:15520..68663hg19UCSC Ensembl
Innerchr5:68520..121663hg18UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg3853029
hg1953144
hg1853144
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5512n100
Supporting Variantsnssv3636503, nssv3636502
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)nsv1029733
Frequency
Sample Size11257
Observed Gain1
Observed Loss1
Observed Complex0
Frequencyn/a


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