A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6499812



Internal ID20873036
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:30877483..30883717hg38UCSC Ensembl
chr16:30888804..30895038hg19UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg386235
hg196235
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18029196
Samples
Known GenesBCL7C
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6499812
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