A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1035094



Internal ID19124313
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:168510020..168543344hg38UCSC Ensembl
Innerchr6:168910700..168944024hg19UCSC Ensembl
Innerchr6:168653549..168686873hg18UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg3833325
hg1933325
hg1833325
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3653072
Samples
Known GenesSMOC2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1035094
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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