A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6049520



Internal ID9115209
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:120509456..120509769hg38UCSC Ensembl
chrX:119643311..119643624hg19UCSC Ensembl
CytobandXq24
Allele length
AssemblyAllele length
hg38314
hg19314
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2661376
Supporting Variants
SamplesHG01113
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6049520
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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