A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6473595



Internal ID9255673
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:26390725..26402931hg38UCSC Ensembl
Outerchr3:26390354..26403301hg38UCSC Ensembl
Innerchr3:26432216..26444422hg19UCSC Ensembl
Outerchr3:26431845..26444792hg19UCSC Ensembl
Cytoband3p24.1
Allele length
AssemblyAllele length
hg3812948
hg1912948
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2669105
Supporting Variants
SamplesNA12156
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6473595
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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