A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1033815



Internal ID19123036
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:44877777..44971062hg38UCSC Ensembl
Innerchr6:44845514..44938799hg19UCSC Ensembl
Innerchr6:44953492..45046777hg18UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg3893286
hg1993286
hg1893286
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3657433
Samples
Known GenesSUPT3H
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1033815
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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