A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5873727



Internal ID22648675
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:102799442..102826581hg38UCSC Ensembl
chrX:102054370..102081509hg19UCSC Ensembl
CytobandXq22.1
Allele length
AssemblyAllele length
hg3827140
hg1927140
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17440345
Samples
Known GenesLINC00630
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5873727
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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