A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5833909



Internal ID9641128
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:7585694..7588372hg38UCSC Ensembl
chr1:7645754..7648432hg19UCSC Ensembl
Cytoband1p36.23
Allele length
AssemblyAllele length
hg382679
hg192679
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2672475
Supporting Variants
SamplesNA19374
Known GenesCAMTA1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5833909
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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