A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4737961



Internal ID20513926
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:44725805..44725877hg38UCSC Ensembl
chr11:44747355..44747427hg19UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg3873
hg1973
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16296260
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4737961
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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