A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1028047



Internal ID18770578
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:167935938..168192818hg38UCSC Ensembl
Innerchr6:168336618..168593498hg19UCSC Ensembl
Innerchr6:168079467..168336347hg18UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg38256881
hg19256881
hg18256881
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6199n100
Supporting Variantsnssv3653024
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)nsv1028047
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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