A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3614237



Internal ID7001132
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:97516458..97518219hg38UCSC Ensembl
Innerchr7:97516458..97518219hg38UCSC Ensembl
Outerchr7:97516344..97518337hg38UCSC Ensembl
chr7:97145770..97147531hg19UCSC Ensembl
Innerchr7:97145770..97147531hg19UCSC Ensembl
Outerchr7:97145656..97147649hg19UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg381762
hg191762
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12903617, essv12903618, essv12903616
SamplesHG00737, HG01889, NA19475
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3614237
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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