A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17445486



Internal ID22503356
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:134612853..134612920hg38UCSC Ensembl
chrX:133746883..133746950hg19UCSC Ensembl
CytobandXq26.3
Allele length
AssemblyAllele length
hg3868
hg1968
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5880663
Supporting Variants
Samples
Known GenesPLAC1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17445486
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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