A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6034402



Internal ID9201464
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:5241431..5246164hg38UCSC Ensembl
chrX:5159472..5164205hg19UCSC Ensembl
CytobandXp22.32
Allele length
AssemblyAllele length
hg384734
hg194734
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2657633
Supporting Variants
SamplesHG01521
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6034402
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