A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5875575



Internal ID22650533
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:44531270..44531357hg38UCSC Ensembl
chrX:44390516..44390603hg19UCSC Ensembl
CytobandXp11.3
Allele length
AssemblyAllele length
hg3888
hg1988
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17458779
Samples
Known GenesFUNDC1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5875575
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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