A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1024995



Internal ID19114213
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:167934598..168196562hg38UCSC Ensembl
Innerchr6:168335278..168597242hg19UCSC Ensembl
Innerchr6:168078127..168340091hg18UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg38261965
hg19261965
hg18261965
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6199n100
Supporting Variantsnssv3652977, nssv3749676, nssv3749677
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)nsv1024995
Frequency
Sample Size11257
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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