A curated catalogue of human genomic structural variation




Variant Details

Variant: essv10561692



Internal ID3735306
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:82606579..82612074hg38UCSC Ensembl
chr2:82833703..82839198hg19UCSC Ensembl
Cytoband2p12
Allele length
AssemblyAllele length
hg385496
hg195496
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3591476
Supporting Variants
SamplesHG03369
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv10561692
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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