A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3732532



Internal ID18684127
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:10469623..10611996hg38UCSC Ensembl
Innerchr21:10900461..11042834hg19UCSC Ensembl
Innerchr21:9922332..10064705hg18UCSC Ensembl
Cytoband21p11.1
Allele length
AssemblyAllele length
hg38142374
hg19142374
hg18142374
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1065873
Supporting Variants
Samples
Known GenesBAGE2, BAGE3, BAGE4, BAGE5, TPTE
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3732532
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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