A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1077212



Internal ID15583712
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:167942096..168149219hg38UCSC Ensembl
Innerchr6:168342776..168549899hg19UCSC Ensembl
Innerchr6:168085625..168292748hg18UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg38207124
hg19207124
hg18207124
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv605398
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)nssv1077212
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