A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5876757



Internal ID22651718
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:16578838..16584167hg38UCSC Ensembl
chrX:16596961..16602290hg19UCSC Ensembl
CytobandXp22.2
Allele length
AssemblyAllele length
hg385330
hg195330
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17430551
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5876757
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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