A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17515512



Internal ID22573474
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:140025919..140039320hg38UCSC Ensembl
chrX:139108078..139121479hg19UCSC Ensembl
CytobandXq27.1
Allele length
AssemblyAllele length
hg3813402
hg1913402
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5970538
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17515512
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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