A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1154907



Internal ID15855038
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:167935400..168193276hg38UCSC Ensembl
Innerchr6:168336080..168593956hg19UCSC Ensembl
Innerchr6:168078929..168336805hg18UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg38257877
hg19257877
hg18257877
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv605385
Supporting Variants
Samples1780862419_A
Known GenesFRMD1, HGC6.3, KIF25, KIF25-AS1, MLLT4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1154907
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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