A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13709375



Internal ID21231155
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:37012987..37012987hg38UCSC Ensembl
chr6:36980763..36980763hg19UCSC Ensembl
Cytoband6p21.2
Allele length
AssemblyAllele length
hg38144
hg19144
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2814132
Supporting Variants
Samples
Known GenesFGD2
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13709375
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.203125


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