A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3611581



Internal ID6651799
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:163556075..163561197hg38UCSC Ensembl
Innerchr6:163556129..163561143hg38UCSC Ensembl
Outerchr6:163556021..163561251hg38UCSC Ensembl
chr6:163977107..163982229hg19UCSC Ensembl
Innerchr6:163977161..163982175hg19UCSC Ensembl
Outerchr6:163977053..163982283hg19UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg385123
hg195123
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12625331
SamplesHG03679
Known GenesQKI
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3611581
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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