A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5883251



Internal ID22658229
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:119939701..119940137hg38UCSC Ensembl
chrX:119073664..119074100hg19UCSC Ensembl
CytobandXq24
Allele length
AssemblyAllele length
hg38437
hg19437
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17431864
Samples
Known GenesNKAP
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5883251
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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