A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17515702



Internal ID22573664
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:154751108..154757229hg38UCSC Ensembl
chrX:153979383..153985504hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg386122
hg196122
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5968633
Supporting Variants
Samples
Known GenesGAB3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17515702
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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