A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3997536



Internal ID18846975
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:3115816..3115877hg38UCSC Ensembl
Outerchr19:3115814..3115875hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg3862
hg1962
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1148747
Supporting Variants
SamplesKWB1
Known GenesGNA11
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nssv3997536
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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