A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1029549



Internal ID19118768
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:15520..82468hg38UCSC Ensembl
Innerchr5:15520..82583hg19UCSC Ensembl
Innerchr5:68520..135583hg18UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg3866949
hg1967064
hg1867064
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5512n100
Supporting Variantsnssv3636516, nssv3636511, nssv3636518, nssv3636515, nssv3636513, nssv3636512, nssv3636517, nssv3636514
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)nsv1029549
Frequency
Sample Size11257
Observed Gain7
Observed Loss1
Observed Complex0
Frequencyn/a


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