A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5878148



Internal ID22653112
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:64044391..64044457hg38UCSC Ensembl
chrX:63264271..63264337hg19UCSC Ensembl
CytobandXq11.2
Allele length
AssemblyAllele length
hg3867
hg1967
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17465222
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5878148
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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