A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5868497



Internal ID22643432
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:64009207..64024278hg38UCSC Ensembl
chrX:63229087..63244158hg19UCSC Ensembl
CytobandXq11.2
Allele length
AssemblyAllele length
hg3815072
hg1915072
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17454845
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5868497
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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