A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6465215



Internal ID9763802
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:132610869..132611298hg38UCSC Ensembl
chrX:131744897..131745326hg19UCSC Ensembl
CytobandXq26.2
Allele length
AssemblyAllele length
hg38430
hg19430
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2664641
Supporting Variants
SamplesNA19720
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6465215
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