A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv956709



Internal ID17305582
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr2:165520706..165520791hg38UCSC Ensembl
Outerchr2:166377216..166377301hg19UCSC Ensembl
Cytoband2q24.3
Allele length
AssemblyAllele length
hg3886
hg1986
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3004015
SamplesBILGI_BIOE
Known GenesCSRNP3
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv956709
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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