A curated catalogue of human genomic structural variation




Variant Details

Variant: essv12605649



Internal ID3906829
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:158655561..158687258hg38UCSC Ensembl
Innerchr6:158655578..158687242hg38UCSC Ensembl
Outerchr6:158655545..158687275hg38UCSC Ensembl
chr6:159076593..159108290hg19UCSC Ensembl
Innerchr6:159076610..159108274hg19UCSC Ensembl
Outerchr6:159076577..159108307hg19UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg3831698
hg1931698
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3611400
Supporting Variants
SamplesHG03559
Known GenesSYTL3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv12605649
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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