A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17448918



Internal ID22506788
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:150975124..150975424hg38UCSC Ensembl
chrX:150143597..150143897hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg38301
hg19301
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5884013
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17448918
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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