A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17516528



Internal ID22574491
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:63463917..63474793hg38UCSC Ensembl
chrX:62683797..62694673hg19UCSC Ensembl
CytobandXq11.1
Allele length
AssemblyAllele length
hg3810877
hg1910877
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5979308
Supporting Variants
Samples
Known GenesLOC92249
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17516528
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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