A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6413971



Internal ID8885566
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:81805917..81811823hg38UCSC Ensembl
OuterchrX:81805396..81812493hg38UCSC Ensembl
InnerchrX:81061416..81067322hg19UCSC Ensembl
OuterchrX:81060895..81067992hg19UCSC Ensembl
CytobandXq21.1
Allele length
AssemblyAllele length
hg387098
hg197098
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2664457
Supporting Variants
SamplesHG00335
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6413971
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