A curated catalogue of human genomic structural variation




Variant Details

Variant: essv7539618



Internal ID10817900
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32018223..32024223hg38UCSC Ensembl
Innerchr6:31986000..31992000hg19UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg386001
hg196001
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3270051
Supporting Variants
SamplesHuRef
Known GenesC4A, C4B, C4B_2
MethodSequencing
Analysis
PlatformComplete Genomics
Comments
ReferencePang_et_al_2013b
Pubmed ID24192839
Accession Number(s)essv7539618
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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