A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3611303



Internal ID6998212
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:153648552..153861919hg38UCSC Ensembl
Innerchr6:153648560..153861912hg38UCSC Ensembl
Outerchr6:153648545..153861927hg38UCSC Ensembl
chr6:153969687..154183054hg19UCSC Ensembl
Innerchr6:153969695..154183047hg19UCSC Ensembl
Outerchr6:153969680..154183062hg19UCSC Ensembl
Cytoband6q25.2
Allele length
AssemblyAllele length
hg38213368
hg19213368
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12592308
SamplesNA19308
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3611303
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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