A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3890901



Internal ID18838611
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:89206381..90025189hg38UCSC Ensembl
Outerchr6:89204468..90033564hg38UCSC Ensembl
Innerchr6:89916100..90734908hg19UCSC Ensembl
Outerchr6:89914187..90743283hg19UCSC Ensembl
Innerchr6:89972819..90791629hg18UCSC Ensembl
Outerchr6:89970906..90800004hg18UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg38829097
hg19829097
hg18829099
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25792024, essv25787997
Samples
Known GenesANKRD6, BACH2, CASP8AP2, GABRR1, GABRR2, GJA10, LYRM2, MDN1, RRAGD, UBE2J1
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Illumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3890901
Frequency
Sample Size3017
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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