A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5977276



Internal ID22752211
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:2149627..2152001hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg382375
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17515967
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5977276
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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