A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5907347



Internal ID22682554
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:88293820..88330755hg38UCSC Ensembl
chr6:89003539..89040474hg19UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg3836936
hg1936936
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17431860
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5907347
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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