A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv955033



Internal ID17303906
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr2:222616993..222617253hg38UCSC Ensembl
Outerchr2:223481712..223481972hg19UCSC Ensembl
Cytoband2q36.1
Allele length
AssemblyAllele length
hg38261
hg19261
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3003763
SamplesBILGI_BIOE
Known GenesFARSB
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv955033
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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