A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv512657



Internal ID15852082
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr22:37509408..37512314hg38UCSC Ensembl
Outerchr22:37905415..37908321hg19UCSC Ensembl
Outerchr22:36235361..36238267hg18UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg382907
hg192907
hg182907
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv625275
Samples1
Known GenesCARD10
MethodSequencing
AnalysisAnalysis of HGMDFN090 by Illumina Genome Analyzer mate pairs
PlatformNot reported
Comments
ReferenceArlt_et_al_2011
Pubmed ID21212237
Accession Number(s)nsv512657
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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