A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3733459



Internal ID18685054
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:44475780..44646211hg38UCSC Ensembl
Innerchr21:45895663..46066128hg19UCSC Ensembl
Innerchr21:44720091..44890556hg18UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg38170432
hg19170466
hg18170466
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1055163
Supporting Variants
Samples
Known GenesC21orf90, KRTAP10-1, KRTAP10-10, KRTAP10-2, KRTAP10-3, KRTAP10-4, KRTAP10-5, KRTAP10-6, KRTAP10-7, KRTAP10-8, KRTAP10-9, MIR7975, TSPEAR, TSPEAR-AS1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3733459
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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