A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4739098



Internal ID20515070
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:99628129..99628249hg38UCSC Ensembl
chr6:100076005..100076125hg19UCSC Ensembl
Cytoband6q16.2
Allele length
AssemblyAllele length
hg38121
hg19121
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16271129
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4739098
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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