A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3957269



Internal ID19218941
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:55651973..55652032hg38UCSC Ensembl
Outerchr5:54947801..54947860hg19UCSC Ensembl
Cytoband5q11.2
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1109697
Supporting Variants
SamplesKWS1
Known GenesSLC38A9
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3957269
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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