A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17515979



Internal ID22573941
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:22477266..22507868hg38UCSC Ensembl
chrX:22495383..22525985hg19UCSC Ensembl
CytobandXp22.11
Allele length
AssemblyAllele length
hg3830603
hg1930603
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5967802
Supporting Variants
Samples
Known GenesLOC100873065
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17515979
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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