A curated catalogue of human genomic structural variation




Variant Details

Variant: essv12312089



Internal ID1215786
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:33956716..33974791hg38UCSC Ensembl
Innerchr6:33957216..33974291hg38UCSC Ensembl
Outerchr6:33955716..33975791hg38UCSC Ensembl
chr6:33924493..33942568hg19UCSC Ensembl
Innerchr6:33924993..33942068hg19UCSC Ensembl
Outerchr6:33923493..33943568hg19UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg3818076
hg1918076
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3608647
Supporting Variants
SamplesHG01080
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv12312089
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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