A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3614428



Internal ID6654634
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:105540104..105540863hg38UCSC Ensembl
Innerchr7:105540112..105540855hg38UCSC Ensembl
Outerchr7:105540096..105540871hg38UCSC Ensembl
chr7:105180551..105181310hg19UCSC Ensembl
Innerchr7:105180559..105181302hg19UCSC Ensembl
Outerchr7:105180543..105181318hg19UCSC Ensembl
Cytoband7q22.3
Allele length
AssemblyAllele length
hg38760
hg19760
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12913832
SamplesHG01746
Known GenesRINT1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3614428
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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