A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3996211



Internal ID19191612
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:186015011..186015088hg38UCSC Ensembl
Outerchr3:185732800..185732877hg19UCSC Ensembl
Cytoband3q27.2
Allele length
AssemblyAllele length
hg3878
hg1978
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1150734
Supporting Variants
SamplesKWB1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nssv3996211
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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