A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1018282



Internal ID18760815
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:168843444..169398234hg38UCSC Ensembl
Innerchr6:169243539..169798329hg19UCSC Ensembl
Innerchr6:168985464..169540254hg18UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg38554791
hg19554791
hg18554791
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6203n100
Supporting Variantsnssv3653079
Samples
Known GenesTHBS2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1018282
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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