A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5634186



Internal ID9325636
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:213397999..213403872hg38UCSC Ensembl
Outerchr1:213397962..213403922hg38UCSC Ensembl
Innerchr1:213571342..213577215hg19UCSC Ensembl
Outerchr1:213571305..213577265hg19UCSC Ensembl
Cytoband1q32.3
Allele length
AssemblyAllele length
hg385961
hg195961
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2664995
Supporting Variants
SamplesNA18519
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5634186
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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