A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3613751



Internal ID6653959
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:76032280..76033713hg38UCSC Ensembl
Innerchr7:76032324..76033670hg38UCSC Ensembl
Outerchr7:76032237..76033757hg38UCSC Ensembl
chr7:75661598..75663031hg19UCSC Ensembl
Innerchr7:75661642..75662988hg19UCSC Ensembl
Outerchr7:75661555..75663075hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg381434
hg191434
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12848281
SamplesHG03771
Known GenesSTYXL1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3613751
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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