A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1027910



Internal ID19117128
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32481746..32562509hg38UCSC Ensembl
Innerchr6:32449523..32530286hg19UCSC Ensembl
Innerchr6:32557501..32638264hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg3880764
hg1980764
hg1880764
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5949n100
Supporting Variantsnssv3745423, nssv3745408, nssv3656042, nssv3745407, nssv3745415, nssv3656048, nssv3656049, nssv3745420, nssv3656044, nssv3656035, nssv3745406, nssv3745412, nssv3656039, nssv3745419, nssv3745421, nssv3656046, nssv3745414, nssv3656043, nssv3656040, nssv3656050, nssv3656045, nssv3656041, nssv3656038, nssv3745418, nssv3656036, nssv3745409, nssv3745413, nssv3745422, nssv3656037, nssv3656051, nssv3745416, nssv3745417, nssv3656047, nssv3745410, nssv3745411
Samples
Known GenesHLA-DRB5, HLA-DRB6
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1027910
Frequency
Sample Size11257
Observed Gain33
Observed Loss2
Observed Complex0
Frequencyn/a


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