A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11074782



Internal ID1076598
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:97762443..97776707hg38UCSC Ensembl
Innerchr3:97762509..97776641hg38UCSC Ensembl
Outerchr3:97762377..97776773hg38UCSC Ensembl
chr3:97481287..97495551hg19UCSC Ensembl
Innerchr3:97481353..97495485hg19UCSC Ensembl
Outerchr3:97481221..97495617hg19UCSC Ensembl
Cytoband3q11.2
Allele length
AssemblyAllele length
hg3814265
hg1914265
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3597102
Supporting Variants
SamplesHG00613
Known GenesARL6
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11074782
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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