A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5977263



Internal ID22752198
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:100994081..101007756hg38UCSC Ensembl
chrX:100249070..100262745hg19UCSC Ensembl
CytobandXq22.1
Allele length
AssemblyAllele length
hg3813676
hg1913676
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17515041
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5977263
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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