A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6106729



Internal ID22015963
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:47608253..47608316hg38UCSC Ensembl
chrX:47467652..47467715hg19UCSC Ensembl
CytobandXp11.23
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17642871
Samples
Known GenesSYN1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6106729
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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