A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6199n100



Internal ID22792286
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:167919247..168211305hg38UCSC Ensembl
chr6:168319927..168611985hg19UCSC Ensembl
chr6:168062776..168354834hg18UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg38292059
hg19292059
hg18292059
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1028529, nsv1026611, nsv1029722, nsv1034831, nsv1025520, nsv1023624, nsv1025498, nsv1019068, nsv1035101, nsv1016308, nsv1018030, nsv1017796, nsv1020358, nsv1016877, nsv1022719, nsv1019817, nsv1028047, nsv1032420, nsv1032706, nsv1033490, nsv1022753, nsv1032453, nsv1021907, nsv1030606, nsv1028031, nsv1019749, nsv1032535, nsv1025733, nsv1026274, nsv1030551, nsv1020162, nsv1027191, nsv1026985, nsv1034898, nsv1027032, nsv1024995, nsv1022991, nsv1018679, nsv1029825, nsv1018856, nsv1026084, nsv1029160, nsv1027944, nsv1022576, nsv1028005, nsv1026853, nsv1020793, nsv1027841, nsv1024875, nsv1021529, nsv1033241, nsv1018414, nsv1032283
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)dgv6199n100
Frequency
Sample Size11257
Observed Gain321
Observed Loss0
Observed Complex0
Frequencyn/a


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