A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3001337



Internal ID17294289
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:13680102..13684601hg38UCSC Ensembl
Outerchr3:13721601..13726100hg19UCSC Ensembl
Cytoband3p25.1
Allele length
AssemblyAllele length
hg384500
hg194500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv955317
Supporting Variants
SamplesBILGI_BIOE
Known GenesLINC00620
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv3001337
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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