A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17851575



Internal ID22035218
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:74548641..74548641hg38UCSC Ensembl
chrX:73768476..73768476hg19UCSC Ensembl
CytobandXq13.2
Allele length
AssemblyAllele length
hg38280
hg19280
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6259531
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17851575
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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