A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1064290



Internal ID18806821
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:36506666..36610835hg38UCSC Ensembl
Innerchr21:37878964..37983133hg19UCSC Ensembl
Innerchr21:36800834..36905003hg18UCSC Ensembl
Cytoband21q22.13
Allele length
AssemblyAllele length
hg38104170
hg19104170
hg18104170
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3600191
Samples
Known GenesCLDN14
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1064290
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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