A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3733453



Internal ID19031734
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:40522282..40594932hg38UCSC Ensembl
Innerchr21:41894209..41966859hg19UCSC Ensembl
Innerchr21:40816079..40888729hg18UCSC Ensembl
Cytoband21q22.2
Allele length
AssemblyAllele length
hg3872651
hg1972651
hg1872651
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1062498
Supporting Variants
Samples
Known GenesDSCAM
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3733453
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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