A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5977057



Internal ID22751992
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:90475088..90477830hg38UCSC Ensembl
chrX:89730087..89732829hg19UCSC Ensembl
CytobandXq21.31
Allele length
AssemblyAllele length
hg382743
hg192743
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17516930
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5977057
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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