A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5884032



Internal ID22659014
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:70903139..70904077hg38UCSC Ensembl
chrX:70122989..70123927hg19UCSC Ensembl
CytobandXq13.1
Allele length
AssemblyAllele length
hg38939
hg19939
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17463190
Samples
Known GenesTEX11
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5884032
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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