A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3649837



Internal ID18601432
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:95485132..95604842hg38UCSC Ensembl
Innerchr6:95933008..96052718hg19UCSC Ensembl
Innerchr6:96039729..96159439hg18UCSC Ensembl
Cytoband6q16.1
Allele length
AssemblyAllele length
hg38119711
hg19119711
hg18119711
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1022589
Supporting Variants
Samples
Known GenesMANEA, MANEA-AS1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3649837
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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