A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1029722



Internal ID18772253
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:167934598..168165463hg38UCSC Ensembl
Innerchr6:168335278..168566143hg19UCSC Ensembl
Innerchr6:168078127..168308992hg18UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg38230866
hg19230866
hg18230866
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6199n100
Supporting Variantsnssv3749622, nssv3655463, nssv3655462
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)nsv1029722
Frequency
Sample Size29084
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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