A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3564842



Internal ID22433566
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:81132103..81132103hg38UCSC Ensembl
chr7:80761419..80761419hg19UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14335094, nssv14335096, nssv14335095
SamplesHG00731, HG00732, HG00733
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3564842
Frequency
Sample Size9
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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