A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17645849



Internal ID21837896
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:123550668..123550668hg38UCSC Ensembl
chrX:122684519..122684519hg19UCSC Ensembl
CytobandXq25
Allele length
AssemblyAllele length
hg38203
hg19203
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6050826
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17645849
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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