A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17647706



Internal ID21839753
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:15433882..15433882hg38UCSC Ensembl
chrX:15452005..15452005hg19UCSC Ensembl
CytobandXp22.2
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6058151
Supporting Variants
Samples
Known GenesPIR, PIR-FIGF
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17647706
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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