A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1022991



Internal ID18765524
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:167929518..168195239hg38UCSC Ensembl
Innerchr6:168330198..168595919hg19UCSC Ensembl
Innerchr6:168073047..168338768hg18UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg38265722
hg19265722
hg18265722
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6199n100
Supporting Variantsnssv3655455, nssv3655454
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)nsv1022991
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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