A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5970580



Internal ID22745515
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:127217169..127243594hg38UCSC Ensembl
chrX:126351152..126377577hg19UCSC Ensembl
CytobandXq25
Allele length
AssemblyAllele length
hg3826426
hg1926426
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17515320
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5970580
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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