A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6084623



Internal ID9459000
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:71948514..71950978hg38UCSC Ensembl
chr13:72522652..72525116hg19UCSC Ensembl
Cytoband13q21.33
Allele length
AssemblyAllele length
hg382465
hg192465
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2660032
Supporting Variants
SamplesNA18909
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6084623
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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