A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5969212



Internal ID22744147
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:56339380..56349124hg38UCSC Ensembl
chrX:56365813..56375557hg19UCSC Ensembl
CytobandXp11.21
Allele length
AssemblyAllele length
hg389745
hg199745
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17516398
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5969212
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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