A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv954339



Internal ID17303213
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:99909942..99910786hg38UCSC Ensembl
Outerchr3:99628786..99629630hg19UCSC Ensembl
Cytoband3q12.1
Allele length
AssemblyAllele length
hg38845
hg19845
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3004472
SamplesBILGI_BIOE
Known GenesCMSS1, FILIP1L, MIR548G
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv954339
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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