A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1033227



Internal ID19122449
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:31103770..31133897hg38UCSC Ensembl
Innerchr6:31071547..31101674hg19UCSC Ensembl
Innerchr6:31179526..31209653hg18UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg3830128
hg1930128
hg1830128
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3655776
Samples
Known GenesC6orf15, CDSN, PSORS1C1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1033227
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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