A curated catalogue of human genomic structural variation




Variant Details

Variant: essv10917556



Internal ID919372
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:9180778..9183532hg38UCSC Ensembl
Innerchr3:9180782..9183528hg38UCSC Ensembl
Outerchr3:9180774..9183536hg38UCSC Ensembl
chr3:9222462..9225216hg19UCSC Ensembl
Innerchr3:9222466..9225212hg19UCSC Ensembl
Outerchr3:9222458..9225220hg19UCSC Ensembl
Cytoband3p25.3
Allele length
AssemblyAllele length
hg382755
hg192755
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3595233
Supporting Variants
SamplesHG03085
Known GenesSRGAP3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv10917556
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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