A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3990926



Internal ID18881679
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:44567119..44567179hg38UCSC Ensembl
Outerchr15:44859317..44859377hg19UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1138363
Supporting Variants
SamplesKWS2
Known GenesSPG11
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3990926
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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