A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15192701



Internal ID21331586
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:47785088..47785088hg38UCSC Ensembl
chr11:47806640..47806640hg19UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg38292
hg19292
Variant TypeCNV insertion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3941445
Supporting Variants
SamplesHG002
Known GenesNUP160
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15192701
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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