A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2656893



Internal ID9576312
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:19934059..19934479hg38UCSC Ensembl
chr19:20044868..20045288hg19UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg38421
hg19421
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6425180, essv5931123, essv6309888, essv6092740, essv5626096, essv5799800, essv5969911, essv6212800, essv5737434, essv5930907, essv5570550, essv6243329, essv6471133, essv6230933, essv6339100, essv5851563, essv6389366, essv5891397, essv6043078, essv6067459, essv5641261, essv6014435, essv6577629, essv5764296, essv6316570
SamplesNA18621, NA18964, NA18530, HG01055, HG00310, HG01389, HG00614, HG01365, NA18546, HG01204, HG00404, HG00319, HG01384, NA19076, HG00472, HG00583, NA18622, NA18990, NA19663, HG00620, NA18620, NA19657, HG00589, HG00611, HG00442
Known GenesZNF93
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2656893
Frequency
Sample Size1151
Observed Gain0
Observed Loss25
Observed Complex0
Frequencyn/a


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