A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4742243



Internal ID20518224
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:7272673..7273359hg38UCSC Ensembl
chr6:7272906..7273592hg19UCSC Ensembl
Cytoband6p24.3
Allele length
AssemblyAllele length
hg38687
hg19687
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16287716
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4742243
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer