A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17456351



Internal ID22514228
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:6160960..6161401hg38UCSC Ensembl
chrX:6079001..6079442hg19UCSC Ensembl
CytobandXp22.31
Allele length
AssemblyAllele length
hg38442
hg19442
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5868368
Supporting Variants
Samples
Known GenesNLGN4X
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17456351
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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