A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3607987



Internal ID6994918
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:5965429..5966562hg38UCSC Ensembl
Innerchr6:5965457..5966534hg38UCSC Ensembl
Outerchr6:5965401..5966590hg38UCSC Ensembl
chr6:5965662..5966795hg19UCSC Ensembl
Innerchr6:5965690..5966767hg19UCSC Ensembl
Outerchr6:5965634..5966823hg19UCSC Ensembl
Cytoband6p25.1
Allele length
AssemblyAllele length
hg381134
hg191134
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12180891, essv12180892, essv12180890, essv12180889
SamplesNA19457, NA19471, NA19031, NA19318
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3607987
Frequency
Sample Size2504
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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