A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4432336



Internal ID21394338
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:30506279..30507457hg38UCSC Ensembl
chr16:30517600..30518778hg19UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg381179
hg191179
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15749738
SamplesSMI018
Known GenesITGAL
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nsv4432336
Frequency
Sample Size15
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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