A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3978766



Internal ID18898595
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:3176062..3176285hg38UCSC Ensembl
Outerchr1:3092626..3092849hg19UCSC Ensembl
Cytoband1p36.32
Allele length
AssemblyAllele length
hg38224
hg19224
Variant TypeCNV tandem duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1142048
Supporting Variants
SamplesKWS2
Known GenesPRDM16
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3978766
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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