A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5907757



Internal ID22682967
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:44978337..44978586hg38UCSC Ensembl
chr11:44999888..45000137hg19UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg38250
hg19250
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17359881
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5907757
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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