A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17737932



Internal ID161598
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:149929000..150341606hg38UCSC Ensembl
chrX:149097218..149509861hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg38412607
hg19412644
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5424262
Supporting Variants
Samples
Known GenesCXorf40B, LINC00894, MIR2114
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17737932
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000626959


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