A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5849961



Internal ID22624896
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:61409302..61410501hg38UCSC Ensembl
chr11:61176774..61177973hg19UCSC Ensembl
Cytoband11q12.2
Allele length
AssemblyAllele length
hg381200
hg191200
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17452218
Samples
Known GenesCPSF7
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5849961
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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