A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17515528



Internal ID22573490
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:140689423..140704841hg38UCSC Ensembl
chrX:139771588..139787006hg19UCSC Ensembl
CytobandXq27.1
Allele length
AssemblyAllele length
hg3815419
hg1915419
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5976755
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17515528
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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