A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3608540



Internal ID6648773
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:31193903..31199261hg38UCSC Ensembl
Innerchr6:31193961..31199204hg38UCSC Ensembl
Outerchr6:31193846..31199319hg38UCSC Ensembl
chr6:31161680..31167038hg19UCSC Ensembl
Innerchr6:31161738..31166981hg19UCSC Ensembl
Outerchr6:31161623..31167096hg19UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg385359
hg195359
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12254285
SamplesNA20527
Known GenesHCG27
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3608540
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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