A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3654330



Internal ID18605925
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:118389935..118578849hg38UCSC Ensembl
Innerchr6:118711098..118900012hg19UCSC Ensembl
Innerchr6:118817791..119006705hg18UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg38188915
hg19188915
hg18188915
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1020586
Supporting Variants
Samples
Known GenesBRD7P3, CEP85L, PLN
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3654330
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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