A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3639295



Internal ID7026078
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:80901550..80920481hg38UCSC Ensembl
chr16:80935447..80954378hg19UCSC Ensembl
Cytoband16q23.2
Allele length
AssemblyAllele length
hg3818932
hg1918932
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv543e214
Supporting Variantsessv15535502, essv15535501, essv15535503
SamplesHG00337, HG00335, HG01077
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3639295
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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