A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17458566



Internal ID22516449
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:50180645..50181776hg38UCSC Ensembl
chrX:49945289..49946418hg19UCSC Ensembl
CytobandXp11.22
Allele length
AssemblyAllele length
hg381132
hg191130
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5868895
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17458566
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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