A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6056751



Internal ID21965985
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:16617994..16617994hg38UCSC Ensembl
chr2:16799262..16799262hg19UCSC Ensembl
Cytoband2p24.2
Allele length
AssemblyAllele length
hg38313
hg19313
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17530668
Samples
Known GenesFAM49A
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6056751
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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