A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4747586



Internal ID20523605
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:121380905..121380965hg38UCSC Ensembl
chr6:121702051..121702111hg19UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16293143
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4747586
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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