A curated catalogue of human genomic structural variation




Variant Details

Variant: essv10961150



Internal ID2072439
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:27251911..27278375hg38UCSC Ensembl
chr3:27293402..27319866hg19UCSC Ensembl
Cytoband3p24.1
Allele length
AssemblyAllele length
hg3826465
hg1926465
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3595665
Supporting Variants
SamplesHG01885
Known GenesNEK10
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv10961150
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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