A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17516047



Internal ID22574009
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:26791048..26803947hg38UCSC Ensembl
chrX:26809165..26822064hg19UCSC Ensembl
CytobandXp21.3
Allele length
AssemblyAllele length
hg3812900
hg1912900
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5978747
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17516047
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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