A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4739449



Internal ID20515422
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:41616308..41616479hg38UCSC Ensembl
chr6:41584046..41584217hg19UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg38172
hg19172
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16284901
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4739449
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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