A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv834090



Internal ID6159814
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr21:37812545..38009542hg19UCSC Ensembl
Outerchr21:36734415..36931412hg18UCSC Ensembl
Outerchr21:36734415..36931412hg17UCSC Ensembl
Cytoband21q22.13
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
hg17n/a
Variant TypeCNV Loss
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusM
Merged Variants
Supporting Variantsnssv1455605, nssv1455604
Samples
Known GenesCLDN14
Method
Analysis
PlatformSMRT Whole Genome Tile Path BAC CGH Array
Comments
ReferenceWong_et_al_2007
Pubmed ID17160897
Accession Number(s)nsv834090
Frequency
Sample Size95
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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