A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3936430



Internal ID21356501
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:87941590..87941662hg38UCSC Ensembl
chr6:88651308..88651380hg19UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg3873
hg1973
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15196896
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3936430
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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