A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3961541



Internal ID19209390
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:75934449..75947749hg38UCSC Ensembl
Outerchr3:75983600..75996900hg19UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg3813301
hg1913301
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1128872
Supporting Variants
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3961541
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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