A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6396659



Internal ID9374062
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:155646791..155651237hg38UCSC Ensembl
OuterchrX:155646634..155651390hg38UCSC Ensembl
InnerchrX:154876452..154880898hg19UCSC Ensembl
OuterchrX:154876295..154881051hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg384757
hg194757
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2662461
Supporting Variants
SamplesHG01140
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6396659
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