A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1060328



Internal ID19149547
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:30363490..30454545hg38UCSC Ensembl
Innerchr21:31735808..31826863hg19UCSC Ensembl
Innerchr21:30657679..30748734hg18UCSC Ensembl
Cytoband21q22.11
Allele length
AssemblyAllele length
hg3891056
hg1991056
hg1891056
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3600116
Samples
Known GenesKRTAP13-1, KRTAP13-2, KRTAP13-3, KRTAP13-4, KRTAP15-1, MIR4327
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1060328
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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