A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2658208



Internal ID9924313
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 Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6408032, essv5692209
SamplesNA19319, HG01455
Known GenesEDA
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2658208
Frequency
Sample Size1151
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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