A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3649847



Internal ID18601442
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:98422726..99818247hg38UCSC Ensembl
Innerchr6:98870602..100266123hg19UCSC Ensembl
Innerchr6:98977323..100372844hg18UCSC Ensembl
Cytoband6q16.1
Allele length
AssemblyAllele length
hg381395522
hg191395522
hg181395522
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1029536
Supporting Variants
Samples
Known GenesCCNC, COQ3, FAXC, FBXL4, PNISR, POU3F2, PRDM13, TSTD3, USP45
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3649847
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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