A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3000815



Internal ID17293767
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr22:43492721..43500320hg38UCSC Ensembl
Outerchr22:43888601..43896200hg19UCSC Ensembl
Cytoband22q13.2
Allele length
AssemblyAllele length
hg387600
hg197600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv955169
Supporting Variants
SamplesBILGI_BIOE
Known GenesMPPED1
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv3000815
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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