A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5849181



Internal ID9692209
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:103452475..103456141hg38UCSC Ensembl
chr7:103092922..103096588hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg383667
hg193667
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2672345
Supporting Variants
SamplesNA19443
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5849181
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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