A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4750826



Internal ID20526686
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:129461573..129461573hg38UCSC Ensembl
chrX:128595550..128595550hg19UCSC Ensembl
CytobandXq25
Allele length
AssemblyAllele length
hg38711
hg19711
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16295777
Samples
Known GenesSMARCA1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4750826
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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