A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15197670



Internal ID21336466
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:105909607..105909662hg38UCSC Ensembl
chr6:106357482..106357537hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3930687
Supporting Variants
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15197670
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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