A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3610375



Internal ID6650601
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:111210614..111215707hg38UCSC Ensembl
Innerchr6:111210614..111215707hg38UCSC Ensembl
Outerchr6:111210526..111215810hg38UCSC Ensembl
chr6:111531817..111536910hg19UCSC Ensembl
Innerchr6:111531817..111536910hg19UCSC Ensembl
Outerchr6:111531729..111537013hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg385094
hg195094
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12503925
SamplesNA18553
Known GenesSLC16A10
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3610375
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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