A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3614074



Internal ID6654281
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:89312637..89479451hg38UCSC Ensembl
chr7:88941951..89108765hg19UCSC Ensembl
Cytoband7q21.13
Allele length
AssemblyAllele length
hg38166815
hg19166815
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12882029, essv12882028
SamplesHG01939, NA19756
Known GenesZNF804B
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3614074
Frequency
Sample Size2504
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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