A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3996191



Internal ID19194780
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:26344958..26345118hg38UCSC Ensembl
Outerchr1:26671449..26671609hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg38161
hg19161
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1150710
Supporting Variants
SamplesKWB1
Known GenesAIM1L
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nssv3996191
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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