A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3890825



Internal ID19185127
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:31995667..32013259hg38UCSC Ensembl
Outerchr6:31983430..32013259hg38UCSC Ensembl
Innerchr6:31963444..31981036hg19UCSC Ensembl
Outerchr6:31951207..31981036hg19UCSC Ensembl
Innerchr6:32071423..32089014hg18UCSC Ensembl
Outerchr6:32059186..32089014hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg3829830
hg1929830
hg1829829
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25786696, essv25780123, essv25787290, essv25780737
Samples
Known GenesC4A, C4B, C4B_2, CYP21A1P, CYP21A2, TNXA, TNXB
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3890825
Frequency
Sample Size3017
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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