A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1148901



Internal ID19201998
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:29622544..29622624hg38UCSC Ensembl
Outerchr19:30113451..30113531hg19UCSC Ensembl
Cytoband19q12
Allele length
AssemblyAllele length
hg3881
hg1981
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3997691
SamplesKWB1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1148901
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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