A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5973998



Internal ID22748933
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:40512391..40521255hg38UCSC Ensembl
chrX:40371643..40380507hg19UCSC Ensembl
CytobandXp11.4
Allele length
AssemblyAllele length
hg388865
hg198865
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17516228
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5973998
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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