A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17439644



Internal ID22497514
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:153769676..153769741hg38UCSC Ensembl
chrX:153035131..153035196hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5874323
Supporting Variants
Samples
Known GenesPLXNB3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17439644
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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