A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3614533



Internal ID7001426
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:110714937..110727417hg38UCSC Ensembl
Innerchr7:110714937..110727417hg38UCSC Ensembl
Outerchr7:110714437..110727917hg38UCSC Ensembl
chr7:110354993..110367473hg19UCSC Ensembl
Innerchr7:110354993..110367473hg19UCSC Ensembl
Outerchr7:110354493..110367973hg19UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg3812481
hg1912481
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12926388, essv12926389
SamplesNA18571, HG03778
Known GenesIMMP2L
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3614533
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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