A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5880282



Internal ID22655252
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:72426665..72426764hg38UCSC Ensembl
chrX:71646515..71646614hg19UCSC Ensembl
CytobandXq13.1
Allele length
AssemblyAllele length
hg38100
hg19100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17460407
Samples
Known GenesHDAC8
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5880282
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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