A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16274408



Internal ID20483626
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:636359..636519hg38UCSC Ensembl
chrX:597094..597254hg19UCSC Ensembl
CytobandXp22.33
Allele length
AssemblyAllele length
hg38161
hg19161
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4758508
Supporting Variants
Samples
Known GenesSHOX
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16274408
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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