A curated catalogue of human genomic structural variation




Variant Details

Variant: essv12410124



Internal ID1665737
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:69492727..69513108hg38UCSC Ensembl
chr6:70202619..70223000hg19UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg3820382
hg1920382
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3609412
Supporting Variants
SamplesHG01527
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv12410124
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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