A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6402n71



Internal ID6324022
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:179220010..179238794hg19UCSC Ensembl
chr5:179152616..179171400hg18UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Loss
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusM
Merged Variants
Supporting Variantsnsv883285, nsv883280
SamplesSP54043, SP54593, SP54967
Known GenesLTC4S, MGAT4B, MIR1229, SQSTM1
Method
Analysis
Platform
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)dgv6402n71
Frequency
Sample Size6533
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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