A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv951996



Internal ID16954183
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:75352960..75364659hg38UCSC Ensembl
Outerchr15:75645301..75657000hg19UCSC Ensembl
Cytoband15q24.2
Allele length
AssemblyAllele length
hg3811700
hg1911700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2999137
SamplesBILGI_BIOE
Known GenesMAN2C1, MIR631, NEIL1
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv951996
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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