A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5692209



Internal ID9185161
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:69787427..69826835hg38UCSC Ensembl
chrX:69007271..69046679hg19UCSC Ensembl
CytobandXq13.1
Allele length
AssemblyAllele length
hg3839409
hg1939409
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2658208
Supporting Variants
SamplesHG01455
Known GenesEDA
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5692209
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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