A curated catalogue of human genomic structural variation




Variant Details

Variant: essv12457599



Internal ID5275408
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:88346809..88425823hg38UCSC Ensembl
chr6:89056528..89135542hg19UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg3879015
hg1979015
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3609881
Supporting Variants
SamplesNA18644
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv12457599
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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