A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3967332



Internal ID19245706
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:126515457..126516757hg38UCSC Ensembl
Outerchr3:126234300..126235600hg19UCSC Ensembl
Cytoband3q21.3
Allele length
AssemblyAllele length
hg381301
hg191301
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1112834
Supporting Variants
SamplesKWS2
Known GenesUROC1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3967332
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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