A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1057981



Internal ID18800512
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:41290295..41422831hg38UCSC Ensembl
Innerchr21:42662222..42794758hg19UCSC Ensembl
Innerchr21:41584092..41716628hg18UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg38132537
hg19132537
hg18132537
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3600210
Samples
Known GenesFAM3B, MX1, MX2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1057981
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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