A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13696929



Internal ID21218787
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:176530237..176530332hg38UCSC Ensembl
chr5:175957238..175957333hg19UCSC Ensembl
Cytoband5q35.2
Allele length
AssemblyAllele length
hg3896
hg1996
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2810610
Supporting Variants
Samples
Known GenesRNF44
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13696929
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.642857


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