A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1025498



Internal ID18768030
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:167952325..168195239hg38UCSC Ensembl
Innerchr6:168353005..168595919hg19UCSC Ensembl
Innerchr6:168095854..168338768hg18UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg38242915
hg19242915
hg18242915
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6199n100
Supporting Variantsnssv3653054, nssv3653053
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)nsv1025498
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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