A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3613706



Internal ID6653915
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:74392112..74392581hg38UCSC Ensembl
Innerchr7:74392142..74392551hg38UCSC Ensembl
Outerchr7:74392082..74392611hg38UCSC Ensembl
chr7:73806442..73806911hg19UCSC Ensembl
Innerchr7:73806472..73806881hg19UCSC Ensembl
Outerchr7:73806412..73806941hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg38470
hg19470
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12843202
SamplesHG00345
Known GenesCLIP2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3613706
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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