A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5969072



Internal ID22744007
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:67406139..67414088hg38UCSC Ensembl
chrX:66625981..66633930hg19UCSC Ensembl
CytobandXq12
Allele length
AssemblyAllele length
hg387950
hg197950
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2281n209
Supporting Variantsnssv17516642
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5969072
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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