A curated catalogue of human genomic structural variation




Variant Details

Variant: essv10922823



Internal ID5928525
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:11430094..11457088hg38UCSC Ensembl
Innerchr3:11430094..11457088hg38UCSC Ensembl
Outerchr3:11429594..11457588hg38UCSC Ensembl
chr3:11471568..11498562hg19UCSC Ensembl
Innerchr3:11471568..11498562hg19UCSC Ensembl
Outerchr3:11471068..11499062hg19UCSC Ensembl
Cytoband3p25.3
Allele length
AssemblyAllele length
hg3826995
hg1926995
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3595292
Supporting Variants
SamplesNA19338
Known GenesATG7
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv10922823
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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