A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5868895



Internal ID22643830
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 StatusM
Merged Variants
Supporting Variantsnssv17458566
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5868895
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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