A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3749561



Internal ID18701156
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 StatusS
Merged Variantsnsv1016522
Supporting Variants
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)nssv3749561
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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