A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17558632



Internal ID21882987
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:37639133..37639191hg38UCSC Ensembl
chr6:37606909..37606967hg19UCSC Ensembl
Cytoband6p21.2
Allele length
AssemblyAllele length
hg3859
hg1959
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6013462
Supporting Variants
Samples
Known GenesMDGA1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17558632
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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