A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17739097



Internal ID162763
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:7002073..7018566hg38UCSC Ensembl
chrX:6920114..6936607hg19UCSC Ensembl
CytobandXp22.31
Allele length
AssemblyAllele length
hg3816494
hg1916494
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5416435
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17739097
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00249844


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