A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6534824



Internal ID8963373
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:142388728..143352799hg38UCSC Ensembl
chrX:141476514..142440592hg19UCSC Ensembl
CytobandXq27.2
Allele length
AssemblyAllele length
hg38964072
hg19964079
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2664441
Supporting Variants
SamplesHG00533
Known GenesSPANXN4
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6534824
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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