A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6600544



Internal ID20973615
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:142870537..142871391hg38UCSC Ensembl
chr6:143191674..143192528hg19UCSC Ensembl
Cytoband6q24.2
Allele length
AssemblyAllele length
hg38855
hg19855
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18140187
Samples
Known GenesHIVEP2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6600544
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