A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5974815



Internal ID22749750
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:39826745..39831880hg38UCSC Ensembl
chrX:39685999..39691134hg19UCSC Ensembl
CytobandXp11.4
Allele length
AssemblyAllele length
hg385136
hg195136
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17516224
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5974815
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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