A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17740355



Internal ID164021
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:64197079..64197158hg38UCSC Ensembl
chrX:63416959..63417038hg19UCSC Ensembl
CytobandXq11.2
Allele length
AssemblyAllele length
hg3880
hg1980
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5415585
Supporting Variants
Samples
Known GenesAMER1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17740355
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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