A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3974332



Internal ID18890550
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:153404559..153404615hg38UCSC Ensembl
Outerchr3:153122348..153122404hg19UCSC Ensembl
Cytoband3q25.2
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1114438
Supporting Variants
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3974332
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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