A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5884909



Internal ID22659893
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:71399612..71399937hg38UCSC Ensembl
chrX:70619462..70619787hg19UCSC Ensembl
CytobandXq13.1
Allele length
AssemblyAllele length
hg38326
hg19326
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17465635
Samples
Known GenesBCYRN1, TAF1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5884909
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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