A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3614185



Internal ID7001080
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:94818052..94827480hg38UCSC Ensembl
Innerchr7:94818088..94827445hg38UCSC Ensembl
Outerchr7:94818017..94827516hg38UCSC Ensembl
chr7:94447364..94456792hg19UCSC Ensembl
Innerchr7:94447400..94456757hg19UCSC Ensembl
Outerchr7:94447329..94456828hg19UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg389429
hg199429
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12897855
SamplesHG00410
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3614185
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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