A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13436662



Internal ID6568154
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:28529033..28685462hg38UCSC Ensembl
chr9:28529031..28685460hg19UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg38156430
hg19156430
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3620168
Supporting Variants
SamplesNA20759
Known GenesLINGO2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13436662
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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