A curated catalogue of human genomic structural variation




Variant Details

Variant: essv12911102



Internal ID1143828
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:101793105..101807310hg38UCSC Ensembl
chr7:101436385..101450590hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg3814206
hg1914206
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3614341
Supporting Variants
SamplesHG00956
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv12911102
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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