A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5883518



Internal ID22658498
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:73844470..73844763hg38UCSC Ensembl
chrX:73064305..73064598hg19UCSC Ensembl
CytobandXq13.2
Allele length
AssemblyAllele length
hg38294
hg19294
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17455539
Samples
Known GenesXIST
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5883518
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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