A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv952025



Internal ID16954212
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:89742870..89762169hg38UCSC Ensembl
Outerchr15:90286101..90305400hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg3819300
hg1919300
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2999169
SamplesBILGI_BIOE
Known GenesMESP1, WDR93
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv952025
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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