A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17445339



Internal ID22503209
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:16721263..16721558hg38UCSC Ensembl
chrX:16739386..16739681hg19UCSC Ensembl
CytobandXp22.2
Allele length
AssemblyAllele length
hg38296
hg19296
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5878717
Supporting Variants
Samples
Known GenesSYAP1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17445339
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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