A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1020362



Internal ID19109581
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:8702116..8747030hg38UCSC Ensembl
Innerchr5:8702228..8747142hg19UCSC Ensembl
Innerchr5:8755228..8800142hg18UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg3844915
hg1944915
hg1844915
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5564n100
Supporting Variantsnssv3639684, nssv3639688, nssv3639678, nssv3639672, nssv3639687, nssv3639671, nssv3639683, nssv3639677, nssv3639674, nssv3639682, nssv3639680, nssv3639676, nssv3639679, nssv3746299, nssv3639686, nssv3746297, nssv3639670, nssv3639681, nssv3639685, nssv3746303, nssv3746298, nssv3746301, nssv3746296, nssv3639675, nssv3639667, nssv3639668, nssv3639669, nssv3639673, nssv3746302, nssv3746300
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)nsv1020362
Frequency
Sample Size11257
Observed Gain0
Observed Loss30
Observed Complex0
Frequencyn/a


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