A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3654378



Internal ID18952659
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:124655521..124706077hg38UCSC Ensembl
Innerchr6:124976667..125027223hg19UCSC Ensembl
Innerchr6:125018366..125068922hg18UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg3850557
hg1950557
hg1850557
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1030013
Supporting Variants
Samples
Known GenesNKAIN2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3654378
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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