A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1077214



Internal ID15583714
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:167942096..168149659hg38UCSC Ensembl
Innerchr6:168342776..168550339hg19UCSC Ensembl
Innerchr6:168085625..168293188hg18UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg38207564
hg19207564
hg18207564
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv605400
Supporting Variants
Samples
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)nssv1077214
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