A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3655386



Internal ID18953667
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:162604329..162751777hg38UCSC Ensembl
Innerchr6:163025361..163172809hg19UCSC Ensembl
Innerchr6:162945351..163092799hg18UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg38147449
hg19147449
hg18147449
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1018573
Supporting Variants
Samples
Known GenesPACRG, PARK2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3655386
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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