A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1016522



Internal ID18759057
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:151412750..151534573hg38UCSC Ensembl
Innerchr6:151733885..151855708hg19UCSC Ensembl
Innerchr6:151775578..151897401hg18UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg38121824
hg19121824
hg18121824
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3749561
Samples
Known GenesC6orf211, CCDC170, RMND1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1016522
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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