A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5972854



Internal ID22747789
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:119189069..119196950hg38UCSC Ensembl
chrX:118323032..118330913hg19UCSC Ensembl
CytobandXq24
Allele length
AssemblyAllele length
hg387882
hg197882
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17515243
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5972854
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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