A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3001391



Internal ID16947657
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:52476885..52530884hg38UCSC Ensembl
Outerchr3:52510901..52564900hg19UCSC Ensembl
Cytoband3p21.1
Allele length
AssemblyAllele length
hg3854000
hg1954000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv954862
Supporting Variants
SamplesBILGI_BIOE
Known GenesNISCH, NT5DC2, STAB1
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv3001391
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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