A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3614164



Internal ID7001059
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:93622605..93628295hg38UCSC Ensembl
Innerchr7:93622605..93628295hg38UCSC Ensembl
Outerchr7:93622512..93628384hg38UCSC Ensembl
chr7:93251917..93257607hg19UCSC Ensembl
Innerchr7:93251917..93257607hg19UCSC Ensembl
Outerchr7:93251824..93257696hg19UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg385691
hg195691
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12891551
SamplesHG02600
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3614164
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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