A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6420231



Internal ID21077784
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 StatusM
Merged Variants
Supporting Variantsnssv18169237
Samples
Known GenesIMPAD1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6420231
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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