A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv958072



Internal ID17306945
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr13:39360087..39361380hg38UCSC Ensembl
Outerchr13:39934224..39935517hg19UCSC Ensembl
Cytoband13q13.3
Allele length
AssemblyAllele length
hg381294
hg191294
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv51n73
Supporting Variantsnssv3004232
SamplesBILGI_BIOE
Known GenesLHFP
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv958072
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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