A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1020162



Internal ID18762698
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:167934598..168171267hg38UCSC Ensembl
Innerchr6:168335278..168571947hg19UCSC Ensembl
Innerchr6:168078127..168314796hg18UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg38236670
hg19236670
hg18236670
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6199n100
Supporting Variantsnssv3655464
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)nsv1020162
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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