A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1028122



Internal ID18770653
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:100326369..100516471hg38UCSC Ensembl
Innerchr6:100774245..100964347hg19UCSC Ensembl
Innerchr6:100880966..101071068hg18UCSC Ensembl
Cytoband6q16.3
Allele length
AssemblyAllele length
hg38190103
hg19190103
hg18190103
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3649854
Samples
Known GenesASCC3, SIM1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1028122
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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