A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17157971



Internal ID21448763
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:168074426..168075067hg38UCSC Ensembl
chr6:168475106..168475747hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg38642
hg19642
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5582820
Supporting Variants
SamplesHG00864
Known GenesFRMD1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17157971
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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