A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17736299



Internal ID159965
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:27645244..27651488hg38UCSC Ensembl
chrX:27663361..27669605hg19UCSC Ensembl
CytobandXp21.3
Allele length
AssemblyAllele length
hg386245
hg196245
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6138262
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17736299
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000628272


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