A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3611218



Internal ID6998129
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:149959367..149964045hg38UCSC Ensembl
Innerchr6:149959375..149964038hg38UCSC Ensembl
Outerchr6:149959360..149964053hg38UCSC Ensembl
chr6:150280503..150285181hg19UCSC Ensembl
Innerchr6:150280511..150285174hg19UCSC Ensembl
Outerchr6:150280496..150285189hg19UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg384679
hg194679
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12581133, essv12581131, essv12581129, essv12581130, essv12581134, essv12581135, essv12581132
SamplesNA18924, NA19119, HG02281, HG03136, NA19206, HG03367, NA19121
Known GenesULBP1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3611218
Frequency
Sample Size2504
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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