A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv951533



Internal ID17300407
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:30996172..31009971hg38UCSC Ensembl
Outerchr10:31285101..31298900hg19UCSC Ensembl
Cytoband10p11.23
Allele length
AssemblyAllele length
hg3813800
hg1913800
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2997925
SamplesBILGI_BIOE
Known GenesZNF438
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv951533
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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