A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv951997



Internal ID16954184
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:75695560..75706959hg38UCSC Ensembl
Outerchr15:75987901..75999300hg19UCSC Ensembl
Cytoband15q24.2
Allele length
AssemblyAllele length
hg3811400
hg1911400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2999138
SamplesBILGI_BIOE
Known GenesCSPG4
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv951997
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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