A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3609542



Internal ID6996463
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:74252686..74262494hg38UCSC Ensembl
Innerchr6:74253186..74261994hg38UCSC Ensembl
Outerchr6:74251686..74263494hg38UCSC Ensembl
chr6:74962402..74972210hg19UCSC Ensembl
Innerchr6:74962902..74971710hg19UCSC Ensembl
Outerchr6:74961402..74973210hg19UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg389809
hg199809
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12429456
SamplesHG02386
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3609542
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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