A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3612276



Internal ID6999177
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:13065570..13175176hg38UCSC Ensembl
Innerchr7:13066070..13174676hg38UCSC Ensembl
Outerchr7:13064570..13176176hg38UCSC Ensembl
chr7:13105195..13214801hg19UCSC Ensembl
Innerchr7:13105695..13214301hg19UCSC Ensembl
Outerchr7:13104195..13215801hg19UCSC Ensembl
Cytoband7p21.3
Allele length
AssemblyAllele length
hg38109607
hg19109607
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12684083
SamplesHG02150
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3612276
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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