A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16265697



Internal ID20474915
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:144373402..144373402hg38UCSC Ensembl
chrX:143456495..143456495hg19UCSC Ensembl
CytobandXq27.3
Allele length
AssemblyAllele length
hg3862
hg1962
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4757185
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16265697
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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