A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1025733



Internal ID18768265
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:167920854..168182912hg38UCSC Ensembl
Innerchr6:168321534..168583592hg19UCSC Ensembl
Innerchr6:168064383..168326441hg18UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg38262059
hg19262059
hg18262059
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6199n100
Supporting Variantsnssv3655446
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)nsv1025733
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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