A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6049159



Internal ID21958393
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:16744707..16744707hg38UCSC Ensembl
chrX:16762830..16762830hg19UCSC Ensembl
CytobandXp22.2
Allele length
AssemblyAllele length
hg38130
hg19130
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17645938
Samples
Known GenesSYAP1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6049159
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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