A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5801538



Internal ID8778941
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:155641695..155958434hg38UCSC Ensembl
chrX:154871356..155188099hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg38316740
hg19316744
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2657377
Supporting Variants
SamplesHG01124
Known GenesSPRY3, VAMP7
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5801538
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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