A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2659036



Internal ID9578455
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:99284003..99344468hg38UCSC Ensembl
chr4:100205160..100265625hg19UCSC Ensembl
Cytoband4q23
Allele length
AssemblyAllele length
hg3860466
hg1960466
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6189143, essv5861771, essv6415275
SamplesNA12842, NA12827, NA12830
Known GenesADH1A, ADH1B, ADH1C, LOC100507053
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2659036
Frequency
Sample Size1151
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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