A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16292788



Internal ID20502006
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:72363697..72364341hg38UCSC Ensembl
chrX:71583547..71584191hg19UCSC Ensembl
CytobandXq13.1
Allele length
AssemblyAllele length
hg38645
hg19645
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4754035
Supporting Variants
Samples
Known GenesHDAC8
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16292788
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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