A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17639819



Internal ID21831866
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:15356451..15362573hg38UCSC Ensembl
chrX:15374573..15380695hg19UCSC Ensembl
CytobandXp22.2
Allele length
AssemblyAllele length
hg386123
hg196123
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6107935
Supporting Variants
Samples
Known GenesFIGF, PIR-FIGF
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17639819
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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