A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3610642



Internal ID6997559
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:123854488..123924229hg38UCSC Ensembl
chr6:124175633..124245374hg19UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg3869742
hg1969742
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12533022
SamplesNA19043
Known GenesNKAIN2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3610642
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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