A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1021529



Internal ID18764063
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:167934598..168172959hg38UCSC Ensembl
Innerchr6:168335278..168573639hg19UCSC Ensembl
Innerchr6:168078127..168316488hg18UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg38238362
hg19238362
hg18238362
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6199n100
Supporting Variantsnssv3749623, nssv3655467, nssv3655465, nssv3655466
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)nsv1021529
Frequency
Sample Size29084
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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