A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1022753



Internal ID18765287
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:167934598..168177306hg38UCSC Ensembl
Innerchr6:168335278..168577986hg19UCSC Ensembl
Innerchr6:168078127..168320835hg18UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg38242709
hg19242709
hg18242709
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6199n100
Supporting Variantsnssv3655468, nssv3655469, nssv3655470, nssv3749624
Samples
Known GenesFRMD1, HGC6.3, KIF25, KIF25-AS1, MLLT4
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1022753
Frequency
Sample Size29084
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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