A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5874861



Internal ID22649815
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:82726866..82732607hg38UCSC Ensembl
chrX:81982315..81988056hg19UCSC Ensembl
CytobandXq21.1
Allele length
AssemblyAllele length
hg385742
hg195742
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2289n209
Supporting Variantsnssv17458805
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5874861
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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