A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6100817



Internal ID9378372
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:15412486..15412688hg38UCSC Ensembl
chrX:15430608..15430810hg19UCSC Ensembl
CytobandXp22.2
Allele length
AssemblyAllele length
hg38203
hg19203
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2669590
Supporting Variants
SamplesNA18571
Known GenesPIR, PIR-FIGF
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6100817
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