A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18169237



Internal ID20736277
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:56992662..56995518hg38UCSC Ensembl
chr8:57905221..57908077hg19UCSC Ensembl
Cytoband8q12.1
Allele length
AssemblyAllele length
hg382857
hg192857
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6420231
Supporting Variants
Samples
Known GenesIMPAD1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18169237
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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