A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1061539



Internal ID18804070
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:43495653..43621943hg38UCSC Ensembl
Innerchr21:44915533..45041824hg19UCSC Ensembl
Innerchr21:43739961..43866252hg18UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg38126291
hg19126292
hg18126292
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3600215, nssv3600216
Samples
Known GenesHSF2BP, MIR6070
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1061539
Frequency
Sample Size29084
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer