A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2813771



Internal ID21259109
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:159816141..159816141hg38UCSC Ensembl
chr6:160237173..160237173hg19UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg38101
hg19101
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13708221
Samples
Known GenesPNLDC1
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2813771
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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