A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17438831



Internal ID22496701
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:143512568..143715773hg38UCSC Ensembl
chrX:142600397..142798867hg19UCSC Ensembl
CytobandXq27.3
Allele length
AssemblyAllele length
hg38203206
hg19198471
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5882617
Supporting Variants
Samples
Known GenesSLITRK4, SPANXN2, SPANXN3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17438831
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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