A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6574926



Internal ID9583252
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:146956692..146960211hg38UCSC Ensembl
chrX:146038210..146041729hg19UCSC Ensembl
CytobandXq27.3
Allele length
AssemblyAllele length
hg383520
hg193520
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2672328
Supporting Variants
SamplesNA19172
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6574926
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