A curated catalogue of human genomic structural variation




Variant Details

Variant: essv12459707



Internal ID3335876
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:89443297..89457105hg38UCSC Ensembl
chr6:90153016..90166824hg19UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg3813809
hg1913809
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3609900
Supporting Variants
SamplesHG02977
Known GenesANKRD6
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv12459707
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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