A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3610277



Internal ID6650503
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:106559337..106560826hg38UCSC Ensembl
Innerchr6:106559337..106560826hg38UCSC Ensembl
Outerchr6:106559259..106560930hg38UCSC Ensembl
chr6:107007212..107008701hg19UCSC Ensembl
Innerchr6:107007212..107008701hg19UCSC Ensembl
Outerchr6:107007134..107008805hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg381490
hg191490
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12498953, essv12498955, essv12498954
SamplesNA19474, NA19020, NA19429
Known GenesAIM1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3610277
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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