A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3620660



Internal ID6660841
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:73148689..73332974hg38UCSC Ensembl
chr9:75763605..75947890hg19UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg38184286
hg19184286
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13518582
SamplesNA18988
Known GenesANXA1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3620660
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer