A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv953634



Internal ID16955821
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr21:42648991..42669590hg38UCSC Ensembl
Outerchr21:44069101..44089700hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg3820600
hg1920600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3000685
SamplesBILGI_BIOE
Known GenesPDE9A
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv953634
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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