A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17515842



Internal ID22573804
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:155978985..155986541hg38UCSC Ensembl
chrX:155208650..155216206hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg387557
hg197557
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5974471
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17515842
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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