A curated catalogue of human genomic structural variation




Variant Details

Variant: essv10972955



Internal ID2027047
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:31987684..31988969hg38UCSC Ensembl
Innerchr3:31987696..31988957hg38UCSC Ensembl
Outerchr3:31987672..31988981hg38UCSC Ensembl
chr3:32029176..32030461hg19UCSC Ensembl
Innerchr3:32029188..32030449hg19UCSC Ensembl
Outerchr3:32029164..32030473hg19UCSC Ensembl
Cytoband3p23
Allele length
AssemblyAllele length
hg381286
hg191286
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3595765
Supporting Variants
SamplesHG01863
Known GenesZNF860
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv10972955
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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