A curated catalogue of human genomic structural variation




Variant Details

Variant: essv12701325



Internal ID2703141
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:22872030..22943285hg38UCSC Ensembl
chr7:22911649..22982904hg19UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg3871256
hg1971256
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3612531
Supporting Variants
SamplesHG02968
Known GenesFAM126A
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv12701325
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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